{"status":"ok","message-type":"work","message-version":"1.0.0","message":{"indexed":{"date-parts":[[2025,10,27]],"date-time":"2025-10-27T20:37:06Z","timestamp":1761597426117},"publisher-location":"Boston, MA","reference-count":134,"publisher":"Springer US","isbn-type":[{"type":"print","value":"9781475790672"},{"type":"electronic","value":"9781475790658"}],"content-domain":{"domain":[],"crossmark-restriction":false},"short-container-title":[],"published-print":{"date-parts":[[1990]]},"DOI":"10.1007\/978-1-4757-9065-8_4","type":"book-chapter","created":{"date-parts":[[2013,5,3]],"date-time":"2013-05-03T17:08:03Z","timestamp":1367600883000},"page":"235-266","source":"Crossref","is-referenced-by-count":17,"title":["Genetic Aspects of Immunoglobulin A Deficiency"],"prefix":"10.1007","author":[{"given":"Charlotte","family":"Cunningham-Rundles","sequence":"first","affiliation":[],"role":[{"role":"author","vocabulary":"crossref"}]}],"member":"297","reference":[{"key":"4_CR1","doi-asserted-by":"crossref","first-page":"1246","DOI":"10.4049\/jimmunol.131.3.1246","volume":"131","author":"M Adachi","year":"1983","unstructured":"Adachi, M., Yodoi, J., Masuda, T., Takatsuki, K., and Uchino, H., 1983, Altered expression of lymphocyte Fc receptor in selective IgA deficiency and IgA nephropathy, J. Immunol. 131: 1246\u20131251.","journal-title":"J. Immunol"},{"key":"4_CR2","doi-asserted-by":"crossref","first-page":"311","DOI":"10.1016\/0090-1229(77)90062-9","volume":"7","author":"M Ambrus","year":"1977","unstructured":"Ambrus, M., Hernadi, E., and Bajtai, G., 1977, Prevalence of HLA-A1 and HLA-B8 antigens in selective IgA deficiency, Clin. Immunol. Immunopathol. 7: 311.","journal-title":"Clin. Immunol. Immunopathol"},{"key":"4_CR3","doi-asserted-by":"crossref","first-page":"223","DOI":"10.1097\/00005792-197105000-00004","volume":"60","author":"AJ Ammann","year":"1971","unstructured":"Ammann, A. J., and Hong, R., 1971, Selective IgA deficiency: Presentation of 30 cases and a review of the literature, Medicine 60: 223.","journal-title":"Medicine"},{"key":"4_CR4","first-page":"260","volume-title":"Immunologic Disorders in Infants and Children, 2nd ed","author":"AJ Ammann","year":"1980","unstructured":"Ammann, A. J., and Hong, R., 1980, Disorders of the IgA system, in: Immunologic Disorders in Infants and Children, 2nd ed. ( R. T. Stiehm and V. Fulginiti, eds.), p. 260, Saunders, Philadelphia."},{"key":"4_CR5","doi-asserted-by":"crossref","first-page":"475","DOI":"10.1016\/0090-1229(77)90011-3","volume":"8","author":"RR Arnold","year":"1977","unstructured":"Arnold, R. R., Cole, M. F., Prince, S., and McGhee, J., 1977, Secretory IgM antibodies to streptococcus mutants in subjects with selective IgA deficiency, Clin. Immunol. Immunopathol. 8: 475\u2013486.","journal-title":"Clin. Immunol. Immunopathol"},{"key":"4_CR6","doi-asserted-by":"crossref","first-page":"379","DOI":"10.1016\/0090-1229(78)90110-1","volume":"9","author":"JS Atwater","year":"1978","unstructured":"Atwater, J. S., and Tomasi, T. B., 1978, Suppressor cells and IgA deficiency, Clin. Immunol. Immunopathol. 9: 379\u2013382.","journal-title":"Clin. Immunol. Immunopathol"},{"key":"4_CR7","doi-asserted-by":"crossref","first-page":"713","DOI":"10.1016\/0091-6749(76)90182-2","volume":"58","author":"J Baker","year":"1976","unstructured":"Baker, J., Hong, R., Dick, E., and Reed, C., 1976, Asthma, IgA deficiency, and respiratory infections, J. Allergy Clin. Immunol. 58: 713.","journal-title":"J. Allergy Clin. Immunol"},{"key":"4_CR8","doi-asserted-by":"crossref","first-page":"316","DOI":"10.3109\/00365516509077057","volume":"17","author":"R Bachmann","year":"1965","unstructured":"Bachmann, R., 1965, Studies on the serum A-globulin level. III. The frequency of a- y-Aglobulinemia, Scand. J. Clin. Lab. Invest. 17: 316.","journal-title":"Scand. J. Clin. Lab. Invest"},{"key":"4_CR9","doi-asserted-by":"crossref","first-page":"307","DOI":"10.1111\/j.1600-0609.1974.tb00214.x","volume":"12","author":"B Beerman","year":"1974","unstructured":"Beerman, B., and Holm, G., 1974, Familial IgA defect, Scand. J. Haematol. 12: 307.","journal-title":"Scand. J. Haematol"},{"key":"4_CR10","doi-asserted-by":"crossref","first-page":"77","DOI":"10.1177\/000992288202100202","volume":"21","author":"PM Blum","year":"1982","unstructured":"Blum, P. M., Stiehm, E. R., and Hong, R., 1982, Spontaneous recovery of selective IgA deficiency: Additional case report and review, Clin. Pediatr. 21: 77\u201380.","journal-title":"Clin. Pediatr"},{"key":"4_CR11","first-page":"55","volume":"6","author":"A Bottaro","year":"1989","unstructured":"Bottaro, A., de Marchi, M., de Lange, G. G., and Carbonara, A. 0., 1989, Human Ig markers, Expl. Clin. Immunogenet. 6: 55\u201359.","journal-title":"Expl. Clin. Immunogenet"},{"key":"4_CR12","first-page":"13","volume":"11","author":"RH Buckley","year":"1975","unstructured":"Buckley, R. H., 1975, Clinical and immunologic features of selective IgA deficiency, Birth Defects: Orig. Artie. Ser. 11: 13.","journal-title":"Birth Defects: Orig. Artie. Ser"},{"key":"4_CR13","doi-asserted-by":"crossref","first-page":"157","DOI":"10.1172\/JCI107906","volume":"55","author":"RH Buckley","year":"1975","unstructured":"Buckley, R. H., and Fiscus, S. A., 1975, Serum IgD and IgE concentrations in immunodeficiency diseases, J. Clin. Invest. 55: 157.","journal-title":"J. Clin. Invest"},{"key":"4_CR14","first-page":"101","volume":"133","author":"GR Burgio","year":"1980","unstructured":"Burgio, G. R., Duse, M., Monafo, V., Ascione, A., and Nespoli, L. 1980, Selective IgA deficiency: Clinical and immunological evaluation of 50 pediatric patients, J. Pediatr. 133: 101\u2013106.","journal-title":"J. Pediatr"},{"key":"4_CR15","first-page":"13","volume":"20","author":"A Carbonara","year":"1986","unstructured":"Carbonara, A. 0., and Demarchi, M., 1986, Ig isotype deficiency caused by gene deletions, Monogr. Allergy 20: 13\u201317.","journal-title":"Ig isotype deficiency caused by gene deletions, Monogr. Allergy"},{"key":"4_CR16","doi-asserted-by":"crossref","first-page":"35","DOI":"10.1016\/S0091-6749(75)80006-6","volume":"55","author":"JT Cassidy","year":"1975","unstructured":"Cassidy, J. T., and Nordby, G. L., 1975, Human serum immunoglobulin concentrations: Prevalence of immunoglobulin deficiencies, J. Allergy Clin. Immunol. 55: 35.","journal-title":"J. Allergy Clin. Immunol"},{"key":"4_CR17","first-page":"275","volume":"280","author":"JT Cassidy","year":"1975","unstructured":"Cassidy, J. T., Burt, A., Petty, R., and Sullivan, D., 1975, Selective IgA deficiency in connective tissue diseases, N. Engl. J. Med. 280: 275.","journal-title":"N. Engl. J. Med"},{"key":"4_CR18","first-page":"296","volume":"35","author":"JT Cassidy","year":"1979","unstructured":"Cassidy, J. T., Oldham, G., and Platts-Mills, T. A. E., 1979, Functional assessment of a B-cell defect in patients with selective IgA deficiency, Clin. Exp. Immunol. 35: 296\u2013299.","journal-title":"Clin. Exp. Immunol"},{"key":"4_CR19","doi-asserted-by":"crossref","first-page":"885","DOI":"10.1378\/chest.73.6.885","volume":"73","author":"CL Casterline","year":"1978","unstructured":"Casterline, C. L., Evans, R., Battista, V. C., and Talamo, R. C., 1978, IgA deficiency and Pi ZZ-antitrypsin deficiency, Chest 73: 885\u2013886.","journal-title":"Chest"},{"key":"4_CR20","first-page":"1164","volume":"37","author":"H Chaabani","year":"1985","unstructured":"Chaabani, H., Bech-Hansen, T., and Cox, D. W., 1985, A multigene deletion within the immunoglobulin heavy chain region, Am. J. Hum. Genet. 37: 1164.","journal-title":"Am. J. Hum. Genet"},{"key":"4_CR21","first-page":"2419","volume":"8","author":"D Choudat","year":"1979","unstructured":"Choudat, D., Taillemite, J. L., Hirsch-Marie, H., Choubrac, P., and Lebas, F. X., 1979, Relation entre isochromosome Xq et deficit serique en immunoglobuline A, Nouvelle Presse Med. 8: 2419.","journal-title":"Nouvelle Presse Med"},{"key":"4_CR22","first-page":"307","volume":"75","author":"HN Claman","year":"1970","unstructured":"Claman, H. N., Merrill, D. A., Peakman, D., and Robinson, A., 1970, Isolated severe gamma-A deficiency: Immunoglobulin levels, clinical disorders, and chromosome studies, J. Lab. Clin. Med. 75: 307\u2013315.","journal-title":"J. Lab. Clin. Med"},{"key":"4_CR23","first-page":"288","volume":"5","author":"LG Cleland","year":"1978","unstructured":"Cleland, L. G., and Bell, D. A., 1978, The occurrence of systemic lupus erythematosus in two kindreds in association with selective IgA deficiency, J. Rheumatol. 5: 288.","journal-title":"J. Rheumatol"},{"key":"4_CR24","doi-asserted-by":"crossref","first-page":"151","DOI":"10.1111\/j.1399-0039.1983.tb01181.x","volume":"22","author":"TJ Cobain","year":"1983","unstructured":"Cobain, T. J., French, M. A. H., Cristiansen, F. T., and Dawkins, R. L., 1983, Association of IgA deficiency with HLA, A28 and B14, Tissue Antigens 22: 151\u2013154.","journal-title":"Tissue Antigens"},{"key":"4_CR25","doi-asserted-by":"crossref","first-page":"76","DOI":"10.1111\/j.1749-6632.1985.tb14593.x","volume":"458","author":"TJ Cobain","year":"1985","unstructured":"Cobain, T. J., Stuckey, M. S., McCluskey, J., Wilton, A., Gedeon, A., Garlepp, M. J., Christiansen, F. T. and Dawkins, R. L., 1985, The coexistence of IgA deficiency and 21-hydroxylase deficiency marked by specific supratypes, Ann. N. Y. Acad. Sci. 458: 76\u201384.","journal-title":"Ann. N. Y. Acad. Sci"},{"key":"4_CR26","first-page":"11","volume":"30","author":"C Collins-Williams","year":"1972","unstructured":"Collins-Williams, C., Kokubu, H. L., Lamenza, C., Nizami, R., Chuiu, A. W., Lewis-McKinley, C., Comerford, T. A., and Varga, E. A., 1972, Incidence of isolated deficiency of IgA in the serum of Canadian children, Ann. Allergy 30: 11.","journal-title":"Ann. Allergy"},{"key":"4_CR27","doi-asserted-by":"crossref","first-page":"495","DOI":"10.1056\/NEJM198108273050905","volume":"305","author":"ME Conley","year":"1981","unstructured":"Conley, M. E., and Cooper, M. D., 1981, Immature IgA B cells in IgA-deficient patients, N. Engl. J. Med. 305: 495.","journal-title":"N. Engl. J. Med"},{"key":"4_CR28","doi-asserted-by":"crossref","first-page":"892","DOI":"10.7326\/0003-4819-106-6-892","volume":"106","author":"ME Conley","year":"1987","unstructured":"Conley, M. E., and Delacroix, D. L., 1987, Intravascular and mucosal immunoglobulin A: Two separate but related systems of immune defence?, Ann. Intern. Med. 106: 892.","journal-title":"Ann. Intern. Med"},{"key":"4_CR29","doi-asserted-by":"crossref","first-page":"977","DOI":"10.1016\/0161-5890(83)90038-X","volume":"20","author":"ME Conley","year":"1983","unstructured":"Conley M. E., Arbeter, A., and Douglas, S. P., 1983, Serum levels of IgA, and IgAZ in children and patients with IgA deficiency, Mol. Immunol. 20: 977\u2013981.","journal-title":"Mol. Immunol"},{"key":"4_CR30","doi-asserted-by":"crossref","first-page":"595","DOI":"10.1016\/0090-1229(80)90155-5","volume":"17","author":"MJ Cowan","year":"1980","unstructured":"Cowan, M. J., Fujiwara, P., Ammann, A. J., 1980, Cellular immune defect in selective IgA deficiency using a microculture method for PHA stimulation and limiting dilution, Clin. Immunol. Immunopathol. 17: 595\u2013605.","journal-title":"Clin. Immunol. Immunopathol"},{"key":"4_CR31","doi-asserted-by":"crossref","first-page":"428","DOI":"10.1038\/297428a0","volume":"297","author":"DW Cox","year":"1982","unstructured":"Cox, D. W., Markovic, V. D., and Teshima, I. E., 1982, Genes for immunoglobulin heavy chains for alpha 1 antitrypsin are localized to specific regions of chromosome 14q, Nature 297: 428\u2013430.","journal-title":"Nature"},{"key":"4_CR32","doi-asserted-by":"crossref","first-page":"119","DOI":"10.1136\/gut.7.2.119","volume":"7","author":"PA Crabb\u00e9","year":"1966","unstructured":"Crabb\u00e9, P. A., and Heremans, J. F., 1966, Lack of gamma A-immunoglobulin in serum of patients with steatorrhea, Gut. 7: 119\u2013125.","journal-title":"Gut"},{"key":"4_CR33","doi-asserted-by":"crossref","first-page":"319","DOI":"10.1016\/0002-9343(67)90031-9","volume":"42","author":"PA Crabb\u00e9","year":"1967","unstructured":"Crabb\u00e9, P. A., and Heremans, J. F., 1967, Selective IgA deficiency with steatorrhea. A new syndrome, Am. J. Med. 42: 319\u2013326.","journal-title":"Am. J. Med"},{"key":"4_CR34","doi-asserted-by":"crossref","first-page":"16","DOI":"10.4049\/jimmunol.132.1.16","volume":"132","author":"SS Crago","year":"1984","unstructured":"Crago, S. S., Kutterh, W. H., Moro, I., Allansmith, M. R., Radl, J., Haaijman, J. J., and Mestecky, J., 1984, Distribution of IgAl, IgAZ and J chain-containing cells in tissues, J. Immunol. 132: 16.","journal-title":"J. Immunol"},{"key":"4_CR35","first-page":"299","volume":"45","author":"C Cunningham-Rundles","year":"1981","unstructured":"Cunningham-Rundles, C., 1981, Autoimmunity in selective IgA deficiency: Relationship to anti-bovine protein antibodies, circulating immune complexes and clinical disease, Clin. Exp. Immunol. 45: 299\u2013304.","journal-title":"Clin. Exp. Immunol"},{"key":"4_CR36","doi-asserted-by":"crossref","first-page":"3880","DOI":"10.4049\/jimmunol.140.11.3880","volume":"140","author":"C Cunningham-Rundles","year":"1988","unstructured":"Cunningham-Rundles, C., and Feng, Z. K., 1988, Analysis of a common inheritable idiotype in IgA-deficient sera using monoclonal antibodies, J. Immunol. 140: 3880\u20133886.","journal-title":"J. Immunol"},{"key":"4_CR37","doi-asserted-by":"crossref","first-page":"270","DOI":"10.1172\/JCI109448","volume":"64","author":"C Cunningham-Rundles","year":"1979","unstructured":"Cunningham-Rundles, C., Brandeis, W. E., Good, R. A., and Day, N. K., 1979, Bovine antigens and the formation of circulating immune complexes in selective IgA deficiency, J. Clin. Invest. 64: 270\u2013272.","journal-title":"J. Clin. Invest"},{"key":"4_CR38","doi-asserted-by":"crossref","unstructured":"Cunningham-Rundles C., Pudifin, D. J., Armstrong, D., and Good, R. A., 1980, Selective IgA deficiency and neoplasia, Vox Sang. 1980: 38\u201361.","DOI":"10.1111\/j.1423-0410.1980.tb02332.x"},{"key":"4_CR39","first-page":"173","volume":"19","author":"C Cunningham-Rundles","year":"1983","unstructured":"Cunningham-Rundles, C., Oxelius, V. A., and Good, R. A., 1983, IgG2 and IgG, subclass deficiencies in selective IgA deficiency in the United States, Birth Defects 19: 173.","journal-title":"Birth Defects"},{"issue":"2","key":"4_CR40","first-page":"383","volume":"47","author":"DL Delacroix","year":"1982","unstructured":"Delacroix, D. L., Dive, C., Rambaud, J. C., and Vaerman, J. P., 1982, IgA subclasses in various secretions and in serum, Immunology 47 (2): 383\u2013385.","journal-title":"Immunology"},{"key":"4_CR41","doi-asserted-by":"crossref","first-page":"617","DOI":"10.4049\/jimmunol.112.2.617","volume":"112","author":"LB Epstein","year":"1974","unstructured":"Epstein, L. B., and Ammann, A. J., 1974, Evaluation of T lymphocyte effector function in immunodeficiency diseases: Abnormalities in mitogen stimulated interferon in patients with selective IgA deficiency, J. Immunol. 112: 617.","journal-title":"J. Immunol"},{"issue":"1","key":"4_CR42","doi-asserted-by":"crossref","first-page":"102","DOI":"10.1136\/jmg.9.1.102","volume":"9","author":"MJ Faed","year":"1972","unstructured":"Faed, M. J., Whyle, R., Patterson, C. R., McCathic, M., and Robertson, J., 1972, Deletion of the long arm of chromosome 18 associated with absence of IgA and hypothyroidism in an adult. J. Med. Genet. 9 (1): 102\u2013105.","journal-title":"J. Med. Genet"},{"key":"4_CR43","doi-asserted-by":"crossref","first-page":"1086","DOI":"10.1016\/S0140-6736(68)91566-3","volume":"2","author":"M Feingold","year":"1968","unstructured":"Feingold, M., and Schwartz, R. S., 1968, IgA and partial deletion of chromosome 18, Lancet 2: 1086.","journal-title":"Lancet"},{"key":"4_CR44","doi-asserted-by":"crossref","first-page":"388","DOI":"10.1136\/jmg.6.4.388","volume":"6","author":"SC Finley","year":"1969","unstructured":"Finley, S. C., Cooper, M. D., Finley, W. H., Uchida, I. A., Noto, T. A., and Roddam, R. F., 1969, Immunological profile in a chromosome 18 deletion syndrome with IgA deficiency, J. Med. Genet. 6: 388.","journal-title":"J. Med. Genet"},{"key":"4_CR45","doi-asserted-by":"crossref","first-page":"93","DOI":"10.1136\/jnnp.41.7.593","volume":"41","author":"A Fontana","year":"1978","unstructured":"Fontana, A., Joller, H., Skvaril, F., and Grob, P., 1978, Immunological abnormalities and HLA antigen frequencies in IgA deficient patients with epilepsy, J. Neurol. Neurosurg. Psychiatry 41: 93.","journal-title":"J. Neurol. Neurosurg. Psychiatry"},{"key":"4_CR46","doi-asserted-by":"crossref","first-page":"513","DOI":"10.1111\/j.1423-0410.1973.tb03545.x","volume":"25","author":"D Frommel","year":"1973","unstructured":"Frommel, D., Moullec, J., Lambin, P., and Fine, J. M., 1973, Selective serum IgA deficiency. Frequency among 15200 French blood donors, Vox Sang. 25: 513\u2013518.","journal-title":"Vox Sang"},{"key":"4_CR47","doi-asserted-by":"crossref","first-page":"565","DOI":"10.1002\/art.1780050605","volume":"5","author":"H Fudenberg","year":"1962","unstructured":"Fudenberg, H., German, J. L., III, and Kunkel, H. G., 1962, The occurrence of rheumatoid factor and other abnormalities in families of patients with agammaglobulinemia, Arthritis Rheumatism 5: 565.","journal-title":"Arthritis Rheumatism"},{"key":"4_CR48","doi-asserted-by":"crossref","first-page":"237","DOI":"10.1159\/000225154","volume":"33","author":"KO Goh","year":"1976","unstructured":"Goh, K. O., Reddy, M. M., and Webb, D. R., 1976, Cancer in a familial IgA deficiency patient: Abnormal chromosomes and B-lymphocytes, Oncology 33: 237.","journal-title":"Oncology"},{"key":"4_CR49","first-page":"204","volume":"72","author":"LS Goldberg","year":"1968","unstructured":"Goldberg, L. S., Barnett, E. V., and Fudenberg, H. H., 1968, Selective absence of IgA: A family study, J. Lab. Clin. Med. 72: 204.","journal-title":"J. Lab. Clin. Med"},{"key":"4_CR50","doi-asserted-by":"crossref","first-page":"344","DOI":"10.1136\/jmg.9.3.344","volume":"9","author":"FJ Grundbacher","year":"1972","unstructured":"Grundbacher, F. J., 1972, Genetic aspects of selective immunoglobulin A deficiency, J. Med. Genet. 9: 344.","journal-title":"J. Med. Genet"},{"key":"4_CR51","doi-asserted-by":"crossref","first-page":"75","DOI":"10.1111\/j.1399-0039.1983.tb00375.x","volume":"21","author":"L Hammarstrom","year":"1983","unstructured":"Hammarstrom, L., and Smith, C. I. E., 1983, HLA-A, B, C and DR antigens in immunoglobulin A deficiency, Tissue Antigens 21: 75\u201379.","journal-title":"Tissue Antigens"},{"key":"4_CR52","doi-asserted-by":"crossref","first-page":"35","DOI":"10.1111\/j.1399-0039.1984.tb00395.x","volume":"24","author":"L Hammarstrom","year":"1984","unstructured":"Hammarstrom, L., Axelsson, V., Bjorkander, J., Hanson, L. A., Moller, E., and Smith, C. I. E., 1984, HLA antigens in selective IgA deficiency, Tissue Antigens 24: 35\u201339.","journal-title":"Tissue Antigens"},{"key":"4_CR53","doi-asserted-by":"crossref","first-page":"778","DOI":"10.1016\/S0140-6736(85)91446-1","volume":"1985","author":"L Hammarstrom","year":"1985","unstructured":"Hammarstrom, L., Ringden, O., Lonngvist, B., Smith, C. I. E., and Wiebe, T., 1985a, Transfer of IgA deficiency to a bone marrow grafted patient with aplastic anemia, Lancet 1985: 778\u2013781.","journal-title":"Lancet"},{"key":"4_CR54","doi-asserted-by":"crossref","first-page":"125","DOI":"10.1111\/j.1744-313X.1985.tb00839.x","volume":"12","author":"L Hammarstrom","year":"1985","unstructured":"Hammarstrom, L., Gubb, R, and Smith, C. I. E., 1985b, Gm allotypes in IgA deficiency, J. Immunogenet. 12: 125\u2013130.","journal-title":"J. Immunogenet"},{"key":"4_CR55","first-page":"661","volume":"60","author":"L Hammarstrom","year":"1985","unstructured":"Hammarstrom, L., Carlsson, B., Smith, C. I. E., and Weislander, L., 1985c, Detection of IgA heavy chain constant region genes in IgA deficient donors: Evidence against gene deletions, Clin. Exp. Immunol. 60: 661\u2013664.","journal-title":"Clin. Exp. Immunol"},{"key":"4_CR56","doi-asserted-by":"crossref","first-page":"197","DOI":"10.1111\/j.1744-313X.1987.tb00381.x","volume":"14","author":"L Hammarstrom","year":"1987","unstructured":"Hammarstrom, L., de Lange, G. G., and Smith, C. I. E., 1987, IgA2 allotypes determined by restriction fragment length polymorphism in IgA deficiency. Re-expression of the silent Atm (2) allotype in the children of IgA deficient patients, J. Immunogenet. 14: 197\u2013201.","journal-title":"J. Immunogenet"},{"key":"4_CR57","doi-asserted-by":"crossref","first-page":"1","DOI":"10.1111\/j.1749-6632.1983.tb26855.x","volume":"409","author":"LA Hanson","year":"1983","unstructured":"Hanson, L. A., Ahlstedt, S., Anderson, B., Carlson, B., Cole, M. F., Cruz, F. R., Dahlgren, U., Ericsson, T. H., Jalil, F., Khan, S. R., Mellander, L., Schneerson, R., SvanborgEden, C., Soderstrom, T., and Wadsworth, C., 1983, Mucosal immunity, Ann. N. Y. Acad. Sci. 409: 1.","journal-title":"Ann. N. Y. Acad. Sci"},{"key":"4_CR58","doi-asserted-by":"crossref","first-page":"280","DOI":"10.1111\/j.1399-0039.1984.tb00046.x","volume":"23","author":"M Heikkila","year":"1984","unstructured":"Heikkila, M., Koistinen, S., Lohman, M., and Koskimies, S., 1984, Increased frequency of HLA-Al and B8 in association with total lack, but not with deficiency of serum IgA, Tissue Antigens 23: 280\u2013283.","journal-title":"Tissue Antigens"},{"key":"4_CR59","doi-asserted-by":"crossref","first-page":"231","DOI":"10.1111\/j.1399-0004.1982.tb01439.x","volume":"22","author":"RP Herrmann","year":"1982","unstructured":"Herrmann, R. P., Chipper, L., and Bell, S., 1982, Chromosome studies in healthy blood donors with IgA deficiency, Clin. Genet. 22: 231\u2013233.","journal-title":"Clin. Genet"},{"key":"4_CR60","first-page":"326","volume":"29","author":"C. C. Huntley","year":"1968","unstructured":"Huntley, C. C., and Stephenson, R. L.,1968, IgA deficiency: Family studies, North Carolina Med. J. 29: 326.","journal-title":"North Carolina Med. J."},{"key":"4_CR61","doi-asserted-by":"crossref","first-page":"199","DOI":"10.1007\/BF00277643","volume":"49","author":"TWJ Hustinx","year":"1979","unstructured":"Hustinx, T. W. J., Scheres, J. M. J. C., Weemaes, C. M. R., terHaar B. G. A., and Janssen, A. H., 1979, Karyotype instability with multiple 7\/14 and 7\/7 rearrangements, Hum. Genet. 49: 199\u2013208.","journal-title":"Hum. Genet"},{"key":"4_CR62","doi-asserted-by":"crossref","first-page":"235","DOI":"10.1007\/BF00914971","volume":"4","author":"T Inoue","year":"1984","unstructured":"Inoue, T., Okubo, H., Kudo, J., Ikuta, T., Hachimine, K., Shibata, R., Yoshinari, D., Fukada, K., and Yanase, T., 1984, Selective IgA deficiency: Analysis of Ig production in vitro, J. Clin. Immunol. 4: 235\u2013241.","journal-title":"in vitro, J. Clin. Immunol"},{"key":"4_CR63","doi-asserted-by":"crossref","first-page":"385","DOI":"10.1016\/0002-9343(81)90164-9","volume":"71","author":"T Iwata","year":"1981","unstructured":"Iwata, T., Incefy, G. S., Cunningham-Rundles, S., et al., 1981, Circulating thymic hormone activity in patients with primary and secondary immunodeficiency diseases, Am. J. Med. 71: 385\u2013394.","journal-title":"Am. J. Med"},{"key":"4_CR64","doi-asserted-by":"crossref","first-page":"80","DOI":"10.1111\/j.1399-0039.1983.tb00376.x","volume":"21","author":"C Jersild","year":"1983","unstructured":"Jersild, C., Staub-Nielsen, L., and Svegaard, A., 1983, HLA and IgA deficiency in blood donors, Tissue Antigens 21: 80.","journal-title":"Tissue Antigens"},{"key":"4_CR65","first-page":"131","volume-title":"Fundamental Immunology","author":"DJ Jeske","year":"1984","unstructured":"Jeske, D. J., and Capra, J. D., 1984, Immunoglobulin structure and function, in: Fundamental Immunology ( W. E. Paul, ed.), pp. 131\u2013165, Raven Press, New York."},{"key":"4_CR66","doi-asserted-by":"crossref","first-page":"81","DOI":"10.1111\/j.1423-0410.1986.tb04851.x","volume":"50","author":"T Kanoh","year":"1986","unstructured":"Kanoh, T., Mizumoto, T., Yasuda, N., Koya, M., Ohno, Y., Uchino, H., Yoshimurac, K., Ohkubo, Y., and Yamaguchi, H., 1986, Selective IgA deficiency in Japanese blood donors: Frequency and statistical analysis, Vox Sang. 50: 81\u201386.","journal-title":"Vox Sang"},{"key":"4_CR67","first-page":"306","volume":"38","author":"MA King","year":"1979","unstructured":"King, M. A., Wells, J. V., and Nelson, D. S., 1979, IgA synthesis by peripheral blood mononuclear cells from normal and selective IgA deficient subjects, Clin. Exp. Immunol. 38: 306\u2013310.","journal-title":"Clin. Exp. Immunol"},{"key":"4_CR68","doi-asserted-by":"crossref","first-page":"427","DOI":"10.1016\/0002-9343(66)90088-X","volume":"41","author":"CH Kirkpatrick","year":"1966","unstructured":"Kirkpatrick, C. H., and Ruth, W. E., 1966, Chronic pulmonary disease and immunologic deficiency, Am. J. Med. 41: 427\u2013432.","journal-title":"Am. J. Med"},{"key":"4_CR69","doi-asserted-by":"crossref","first-page":"192","DOI":"10.1111\/j.1423-0410.1975.tb00494.x","volume":"29","author":"J Koistinen","year":"1975","unstructured":"Koistinen, J., 1975, Selective IgA deficiency in blood donors, Vox Sang. 29: 192.","journal-title":"Vox Sang"},{"key":"4_CR70","doi-asserted-by":"crossref","first-page":"181","DOI":"10.1111\/j.1423-0410.1976.tb02811.x","volume":"30","author":"J Koistinen","year":"1976","unstructured":"Koistinen, J., 1976, Familial clustering of selective IgA deficiency, Vox Sang. 30: 181\u2013190.","journal-title":"Vox Sang"},{"key":"4_CR71","first-page":"198","volume":"50","author":"AO Kwitko","year":"1982","unstructured":"Kwitko, A. O., Roberts-Thomas, P. J., and Shearman, D. J. C., 1982, Low molecular weight IgM in selective IgA deficiency, Clin. Exp. Immunol. 50: 198\u2013202.","journal-title":"Clin. Exp. Immunol"},{"key":"4_CR72","doi-asserted-by":"crossref","first-page":"461","DOI":"10.1016\/S0025-6196(12)65643-2","volume":"63","author":"S Lakhanpal","year":"1988","unstructured":"Lakhanpal, S., O\u2019Duffy, J. D., Homburg, H. A., and Moore, S. B., 1988, Evidence for linkage of IgA deficiency with the major histocompatibility complex, Mayo Clin. Proc. 63: 461\u2013465.","journal-title":"Mayo Clin. Proc"},{"key":"4_CR73","first-page":"26","volume":"80","author":"AR Lawton","year":"1972","unstructured":"Lawton, A. R., Royal, S. A., Self, K. S., and Cooper, M. D., 1972, IgA determinants on B lymphocytes in patients with deficiency of circulating IgA, J. Lab. Clin. Med. 80: 26.","journal-title":"J. Lab. Clin. Med"},{"key":"4_CR74","doi-asserted-by":"crossref","first-page":"320","DOI":"10.1136\/adc.48.4.320","volume":"48","author":"J Leisti","year":"1973","unstructured":"Leisti, J., Leisti, S., Perheentupa, J., Savilahti, E., and Aula, P. 1973, Absence of IgA and growth hormone deficiency associated with a short arm deletion of chromosome 18, Arch. Dis. Child. 48: 320.","journal-title":"Arch. Dis. Child"},{"key":"4_CR75","doi-asserted-by":"crossref","first-page":"760","DOI":"10.1038\/300760a0","volume":"300","author":"MP Franc","year":"1982","unstructured":"Le Franc, M. P., Le Franc, G., and Rabbits, T. M., 1982, Inherited deletion of immunoglobulin heavy chain constant region genes in normal human individuals, Nature 300: 760\u2013762.","journal-title":"Nature"},{"key":"4_CR76","first-page":"207","volume":"1","author":"MP Lefranc","year":"1983","unstructured":"LeFranc, M. P., LeFranc, G., De Lange, G., Out, T. A., van Denbroek, P. J., van Nieuwkoop, J., Radl, J., Helal, A. N., Chabaani, H., van Loghem, E., and Rabbits, T. H., 1983, Instability of the human immunoglobulin heavy chain constant region locus indicated by different inherited chromosomal deletions, Mol. Biol. Med. 1: 207\u2013217.","journal-title":"Mol. Biol. Med"},{"key":"4_CR77","doi-asserted-by":"crossref","first-page":"418","DOI":"10.1016\/S0022-3476(82)80447-2","volume":"100","author":"AB Leong","year":"1982","unstructured":"Leong, A. B., Gange, R. W., and O\u2019Connor, R. D., 1982, Twenty nail dystrophy associated with selective IgA deficiency, J. Pediatr. 100: 418\u2013419.","journal-title":"J. Pediatr"},{"key":"4_CR78","doi-asserted-by":"crossref","first-page":"52","DOI":"10.1016\/S0022-3476(81)80532-X","volume":"98","author":"D Levitt","year":"1981","unstructured":"Levitt, D., and Cooper, M. D., 1981, Immunoregulatory defects in a family with selective IgA deficiency, J. Pediatr. 98: 52\u201358.","journal-title":"J. Pediatr"},{"key":"4_CR79","doi-asserted-by":"crossref","first-page":"453","DOI":"10.1136\/jmg.17.6.453","volume":"17","author":"RM Lewkonia","year":"1980","unstructured":"Lewkonia, R. M., Lin, C. C., and Haslam, R. H. A., 1980, Selective IgA deficiency with 18q + and 18q \u2014 karyotypic anomalies, J. Med. Genet. 17: 453\u2013456.","journal-title":"J. Med. Genet"},{"key":"4_CR80","first-page":"932","volume":"120","author":"DM Mccarthy","year":"1978","unstructured":"McCarthy, D. M., Katz. S. I., Gazze, L., Waldmann, T. A., Nelsor, D. L., and Strober, W., 1978, Selective IgA deficiency associated with total villous atrophy of the small intestine and an organ-specific anti-epithelial cell antibody, J. Immunol. 120: 932.","journal-title":"Selective IgA deficiency associated with total villous atrophy of the small intestine and an organ-specific anti-epithelial cell antibody, J. Immunol"},{"key":"4_CR81","first-page":"103","volume":"25","author":"DBL Mccleland","year":"1979","unstructured":"McCleland, D. B. L., Shearman, D. J., and Van Furth, R., 1979, Synthesis of immunoglobulin and secretory components by gastrointestinal mucosa in patients with hypogammaglobulinemia or IgA deficiency, Clin. Exp. Immunol. 25: 103.","journal-title":"Clin. Exp. Immunol"},{"key":"4_CR82","doi-asserted-by":"crossref","first-page":"175","DOI":"10.1007\/BF00916814","volume":"9","author":"JR Mcghee","year":"1989","unstructured":"McGhee, J. R., Mestecky, J., Elson, C. O., and Kiyono, H., 1989, Regulation of IgA synthesis and immune response by T cells and interleukins, J. Clin. Immunol. 9: 175.","journal-title":"J. Clin. Immunol"},{"key":"4_CR83","doi-asserted-by":"crossref","first-page":"153","DOI":"10.1016\/S0065-2776(08)60240-0","volume":"40","author":"J Mestecky","year":"1987","unstructured":"Mestecky, J., and McGhee, J. R., 1987, Immunoglobulin A (IgA): Molecular and cellular interactions involved in IgA biosynthesis and immune response, Adv. Immunol. 40: 153.","journal-title":"Adv. Immunol"},{"key":"4_CR84","doi-asserted-by":"crossref","first-page":"5811","DOI":"10.1073\/pnas.81.18.5811","volume":"81","author":"N Migone","year":"1984","unstructured":"Migone, N., Olivero, S., De Lange, G., Delacroix, D. L., Boschis, D., Altruda, F., Silengo, L., Demarchi, M., and Carbonara, A. 0., 1984, Multiple gene deletions within the human immunoglobulin heavy chain cluster, Proc. Nat. Acad. Sci. USA 81: 5811.","journal-title":"Proc. Nat. Acad. Sci. USA"},{"key":"4_CR85","doi-asserted-by":"crossref","first-page":"37","DOI":"10.1038\/308037a0","volume":"308","author":"KE Mostov","year":"1984","unstructured":"Mostov, K. E., Friedlander, M., and Blobel, G., 1984, The receptor for transepithelial transport of IgA and IgM contains multiple immunoglobulin-like domains, Nature 308: 37.","journal-title":"Nature"},{"key":"4_CR86","first-page":"229","volume":"8","author":"JB Natvig","year":"1971","unstructured":"Natvig, J. B., Harboe, M., Fausa, O., and Tveit, A., 1971, Family studies in individuals with selective absence of A-globulin, Clin. Exp. Immunol. 8: 229.","journal-title":"Clin. Exp. Immunol"},{"key":"4_CR87","doi-asserted-by":"crossref","first-page":"71","DOI":"10.1542\/peds.49.1.71","volume":"49","author":"PA Nell","year":"1972","unstructured":"Nell, P. A., Ammann, A. J., Hong, R., and Stiehm, E. R., 1972, Familial selective IgA deficiency, Pediatrics 49: 71.","journal-title":"Pediatrics"},{"key":"4_CR88","doi-asserted-by":"crossref","first-page":"174","DOI":"10.1111\/j.1399-0039.1982.tb01437.x","volume":"19","author":"K Oen","year":"1982","unstructured":"Oen, K., Petty, R. E., and Schroeder, M. L., 1982, Immunoglobulin A deficiency in genetic studies, Tissue Antigens 19: 174\u2013182.","journal-title":"Tissue Antigens"},{"key":"4_CR89","doi-asserted-by":"crossref","first-page":"184","DOI":"10.1111\/j.1399-0004.1977.tb01297.x","volume":"11","author":"K Ogata","year":"1977","unstructured":"Ogata, K., Iinuma, K., Kamimura, K., Morinaga, R., and Kato, J., 1977, A case report of a presumptive +i(18p) associated with serum IgA deficiency, Clin. Genet. 11: 184\u2013188.","journal-title":"Clin. Genet"},{"key":"4_CR90","first-page":"1476","volume":"304","author":"VA Oxelius","year":"1981","unstructured":"Oxelius, V. A., Laurell, A. B., Linguist, B., Golebiowska, H., Axelsson, U., Bjorkander, J., and Hanson, L. A., 1981, IgG subclasses in selective IgA deficiency, N. Engl. J. Med. 304: 1476.","journal-title":"Med"},{"key":"4_CR91","doi-asserted-by":"crossref","first-page":"509","DOI":"10.1001\/archinte.141.4.509","volume":"141","author":"F Perez-Jiminez","year":"1981","unstructured":"Perez-Jiminez, F., Lopez, P. B., Tallo, E. P., Guzman, J. R., Molina, J. S., and Perez-Perez, J. A., 1981, Selective IgA deficiency and the HLA-B8 antigen, Arch. Intern. Med. 141: 509\u2013510.","journal-title":"Arch. Intern. Med"},{"key":"4_CR92","doi-asserted-by":"crossref","first-page":"1620","DOI":"10.1056\/NEJM198512263132602","volume":"313","author":"RE Petty","year":"1985","unstructured":"Petty, R. E., Sherry, D. D., and Johannson, J., 1985, Anti-antibodies in pregnancy, N. Engl. J. Med. 313: 1620\u20131625.","journal-title":"N. Engl. J. Med"},{"key":"4_CR93","first-page":"1103","volume":"190","author":"AG Plaut","year":"1975","unstructured":"Plaut, A. G., Gilbert, J. V., Arlenstein, M. S., and Capra, J. D., 1975, Neisseria gonorrhoeae and Neisseria meningitides: Extracellular enzyme cleaves human immunoglobulin. A. Science 190: 1103\u20131105.","journal-title":"Neisseria gonorrhoeae and Neisseria meningitides: Extracellular enzyme cleaves human immunoglobulin. A. Science"},{"key":"4_CR94","first-page":"689","volume":"53","author":"A Plebani","year":"1983","unstructured":"Plebani, A., Mira, E., Mevio, E., Monafo, V., Notarangelo, L. D., Avanzini, A., and Ugazio, A. G., 1983, IgM and IgD concentrations in the serum and secretions of children with selective IgA deficiency, Clin. Exp. Immunol. 53: 689\u2013696.","journal-title":"Clin. Exp. Immunol"},{"key":"4_CR95","doi-asserted-by":"crossref","first-page":"804","DOI":"10.1016\/S0140-6736(76)90641-3","volume":"2","author":"W Proesman","year":"1976","unstructured":"Proesman, W., Jaeken, J., and Eeckels, R., 1976, D-Penicillamine-induced IgA deficiency in Wilson\u2019s disease, Lancet [letter] 2: 804.","journal-title":"Lancet"},{"key":"4_CR96","first-page":"20","volume":"63","author":"JH Rockey","year":"1964","unstructured":"Rockey, J. H., Hanson, L. A., Heremans, J. F., and Kundel, H. G., 1964, Beta-2\/Agammaglobulinemia in two healthy men, J. Lab. Clin. Med. 63: 20.","journal-title":"J. Lab. Clin. Med"},{"key":"4_CR97","first-page":"1459","volume":"78","author":"F Rosner","year":"1978","unstructured":"Rosner, F., Vallejo, V., Khan, F. A., Wessely, Z., Grunwald, H. W., and Calas, C., 1978, Hypogammaglobulinemia and selective immunoglobulin A deficiency. Double consanguinity in family, N.Y. State J. Med. 78: 1459.","journal-title":"N.Y. State J. Med"},{"key":"4_CR98","doi-asserted-by":"crossref","first-page":"964","DOI":"10.1016\/S0022-3476(69)80234-9","volume":"74","author":"RHA Ruvalcaba","year":"1969","unstructured":"Ruvalcaba, R. H. A., and Thuline, H. C., 1969, IgA absence associated with short arm deletion of chromosome No. 18, J. Pediatr. 74: 964\u2013965.","journal-title":"J. Pediatr"},{"key":"4_CR99","first-page":"257","volume-title":"Progress in Immunodeficiency research and Therapy","author":"E Savilahti","year":"1984","unstructured":"Savilahti, E., Eskola, J. and Koskimies, S., 1984, IgA deficiency in coeliac disease, in: Progress in Immunodeficiency research and Therapy ( C. Griscelli and J. Vossen eds.), pp. 257\u2013259, Elsevier Science Publishers, Amsterdam."},{"key":"4_CR100","doi-asserted-by":"crossref","first-page":"8015","DOI":"10.1073\/pnas.86.20.8015","volume":"86","author":"FM Schaffer","year":"1989","unstructured":"Schaffer, F. M., Palermos, J., Zhu, Z. B., Barger, B. O., Cooper, M. D., and Volanakis. J. E., 1989, Individuals with IgA deficiency and common variable immunodeficiency share polymorphisms of major histocompatibility complex class III genes, Proc. Natl. Acad. Sci. USA 86: 8015\u20138019.","journal-title":"Proc. Natl. Acad. Sci. USA"},{"key":"4_CR101","volume-title":"Blackwell Scientific Publications","author":"MS Schanfield","year":"1986","unstructured":"Schanfield, M. S., and van Loghem, E., 1986, Human immunoglobulin allotypes, in: Handbook of Experimental Immunology (D. M. Wien et al., eds.), Vol. 3, Chapter 94, Blackwell Scientific Publications."},{"key":"4_CR102","first-page":"173","volume":"9","author":"MS Scotta","year":"1982","unstructured":"Scotta, M. S., Maggiore, G., DeGiacomo, C., Martini, A., Burgio, V. L., and Ugazio, A. G., 1982, IgA containing plasma cells in the intestinal mucosa of children with selective IgA deficiency, J. Clin. Lab. Immunol. 9: 173\u2013175.","journal-title":"J. Clin. Lab. Immunol"},{"key":"4_CR103","doi-asserted-by":"crossref","first-page":"632","DOI":"10.1016\/S0140-6736(75)90115-4","volume":"2","author":"J Seager","year":"1975","unstructured":"Seager, J., Jamison, D. L., Wilson, J., Wilson, J., Hayward, A. R., and Soothill, J. F., 1975, IgA deficiency, epilepsy and phenytoin treatment, Lancet 2: 632.","journal-title":"Lancet"},{"key":"4_CR104","doi-asserted-by":"crossref","first-page":"753","DOI":"10.1016\/S0338-4535(78)80013-0","volume":"21","author":"J Seignalet","year":"1978","unstructured":"Seignalet, J., Michael, F. B., Guendon, R., Thomas, R., Robinet-Levy, M., and Lapinski, H., 1978, HLA et deficit en IgA, Rev. Fr. Transfusion Immunohematol. 21: 753.","journal-title":"Rev. Fr. Transfusion Immunohematol"},{"key":"4_CR105","doi-asserted-by":"crossref","first-page":"212","DOI":"10.1016\/0090-1229(73)90021-4","volume":"1","author":"HKB Silver","year":"1973","unstructured":"Silver, H. K. B., Shuster, J., Gold, P., Hawkins, D., and Freedman, S. 0., 1973, Endo-crinopathy and IgA deficiency, Clin. Immunol. Immunopathol. 1: 212.","journal-title":"Clin. Immunol. Immunopathol"},{"key":"4_CR106","first-page":"225","volume-title":"Progress in Immunodeficiency Research and Therapy","author":"CIE Smith","year":"1986","unstructured":"Smith, C. I. E., and Hammarstrom, L., 1986a, Transcription of immunoglobulin C a-genes in individuals with IgA deficiency, in: Progress in Immunodeficiency Research and Therapy ( J. Vossen and C. Griscelli, eds.), pp. 225\u2013259, Elsevier, New York."},{"key":"4_CR107","first-page":"18","volume":"20","author":"C. I. E. Smith","year":"19866","unstructured":"Smith, C. I. E., and Hammarstrom, L., 19866, Detection of immunoglobulin genes in individuals with immunoglobulin class or subclass deficiency; evidence for a pretranslational defect, Monogr. Allergy 20: 18\u201323.","journal-title":"Monogr. Allergy"},{"key":"4_CR108","doi-asserted-by":"crossref","first-page":"1092","DOI":"10.2337\/diab.27.11.1092","volume":"27","author":"WI Smith","year":"1978","unstructured":"Smith, W. I., Rabin, B. S., Huelimantel, A., Van Thiel, D. H., and Drash, A., 1978, Immunopathology of juvenile-onset diabetes mellitus I. IgA deficiency and juvenile diabetes, Diabetes 27: 1092.","journal-title":"Diabetes"},{"key":"4_CR109","doi-asserted-by":"crossref","first-page":"325","DOI":"10.1016\/0090-1229(82)90197-0","volume":"25","author":"O Stannegard","year":"1983","unstructured":"Stannegard, O., Bjorkander, J., Hanson, L. A., and Hermodsson, S., 1983, Natural killer cells in common variable immunodeficiency and selective IgA deficiency, Clin. Immunol. Immunopathol. 25: 325\u2013334.","journal-title":"Clin. Immunol. Immunopathol"},{"key":"4_CR110","doi-asserted-by":"crossref","first-page":"11","DOI":"10.1136\/jmg.7.1.11","volume":"7","author":"JM Stewart","year":"1970","unstructured":"Stewart, J. M., Go, S., Ellis, E., and Robinson, A., 1970, Absent IgA and deletions of chromosome 18, J. Med. Genet. 7: 11\u201319.","journal-title":"J. Med. Genet"},{"key":"4_CR111","doi-asserted-by":"crossref","first-page":"585","DOI":"10.1136\/adc.43.231.585","volume":"43","author":"F. Stocker","year":"1988","unstructured":"Stocker, F., Ammann, P., and Rossi, E., 1988, selective y-A-Globulin deficiency, with dominant autosomal inheritance in a Swiss family, Arch. Dis. Child. 43: 585.","journal-title":"Arch. Dis. Child."},{"key":"4_CR112","doi-asserted-by":"crossref","first-page":"1359","DOI":"10.1001\/jama.1982.03330110055029","volume":"248","author":"RB Stricker","year":"1982","unstructured":"Stricker, R. B., and Linnker, C. A., 1982, Pernicious anemia, 18q deletion syndrome and IgA deficiency, J. Am. Med. Assoc. 248: 1359\u20131360.","journal-title":"J. Am. Med. Assoc"},{"key":"4_CR113","doi-asserted-by":"crossref","first-page":"289","DOI":"10.1016\/0198-8859(86)90056-X","volume":"16","author":"R Strothman","year":"1986","unstructured":"Strothman, R., White, M. B., Testin, J., Chen, S. N., and Ball, M. S., 1986, HLA and IgA deficiency in blood donors, Hum. Immunol. 16: 289\u2013294.","journal-title":"Hum. Immunol"},{"key":"4_CR114","doi-asserted-by":"crossref","first-page":"81","DOI":"10.1111\/j.1399-0004.1987.tb03330.x","volume":"32","author":"RDFM Taalman","year":"1987","unstructured":"Taalman, R. D. F. M., Weemaes, C. M. R., Hustinx, T. W. J., Scheres, J. M. J. C., Clement, J. M. E., and Stoelinga, G. B. A., 1987, Chromosome studies in IgA-deficient patients, Clin. Genet. 32: 81\u201387.","journal-title":"Clin. Genet"},{"key":"4_CR115","doi-asserted-by":"crossref","first-page":"127","DOI":"10.1007\/BF00287166","volume":"51","author":"L Tiepolo","year":"1979","unstructured":"Tiepolo, L., Maraschio, P., Gimeli, G., Cuoco, C., Gargani, G. F., and Romano, C., 1979, Multibranched chromosomes 1,9, and 16 in a patient with combined IgA and IgE deficiency, Hum. Genet. 51: 127.","journal-title":"Hum. Genet"},{"key":"4_CR116","doi-asserted-by":"crossref","first-page":"1","DOI":"10.1016\/S0065-2776(08)60441-1","volume":"9","author":"TB Tomasi","year":"1968","unstructured":"Tomasi, T. B., and Bienenstock, J., 1968, Secretory immunoglobulins, Adv. Immunol. 9: 1.","journal-title":"Adv. Immunol"},{"key":"4_CR117","doi-asserted-by":"crossref","first-page":"124","DOI":"10.1016\/S0140-6736(71)92302-6","volume":"2","author":"GH Tomkin","year":"1971","unstructured":"Tomkin, G. H., Machinney, H., and Nevin, N. C., 1971, Isolated absence of IgA with autosomal dominant inheritance, Lancet 2: 124.","journal-title":"Lancet"},{"key":"4_CR118","doi-asserted-by":"crossref","first-page":"311","DOI":"10.1097\/00000441-197805000-00008","volume":"275","author":"SH Tsung","year":"1978","unstructured":"Tsung, S. H., and Ajlouni, K., 1978, Immune competence in patients with Klinefelter syndrome, Am. J. Med. Sci. 275: 311\u2013317.","journal-title":"Am. J. Med. Sci"},{"key":"4_CR119","doi-asserted-by":"crossref","first-page":"1104","DOI":"10.1073\/pnas.76.3.1104","volume":"76","author":"Y Tsuzukida","year":"1979","unstructured":"Tsuzukida, Y., Wang, C., and Putnam, F. W., 1979, Structure of the A2m(1) allotype of human IgA-A recombinant molecule, Proc. Natl. Acad. Sci. USA 76: 1104.","journal-title":"Proc. Natl. Acad. Sci. USA"},{"key":"4_CR120","first-page":"425","volume":"14","author":"JP Vaerman","year":"1968","unstructured":"Vaerman, J. P., Heremans, J. F., and Laurell, C. B., 1968, Distribution of alpha chain subclass in normal and pathological IgA-globulins, Immunology 14: 425\u2013432.","journal-title":"Immunology"},{"key":"4_CR121","doi-asserted-by":"crossref","first-page":"57","DOI":"10.1002\/eji.1830040115","volume":"4","author":"E Loghem","year":"1974","unstructured":"Van Loghem, E., 1974, Familial occurrence of isolated IgA deficiency associated with antibodies to IgA. Evidence against a structural gene defect, Eur. J. Immunol. 4: 57.","journal-title":"Eur. J. Immunol"},{"key":"4_CR122","doi-asserted-by":"crossref","first-page":"481","DOI":"10.1111\/j.1423-0410.1973.tb03490.x","volume":"24","author":"E Loghem","year":"1973","unstructured":"Van Loghem, E., Wang, A. C., and Shuster, J., 1973, A new genetic marker of human immunoglobulin determined by an allele at the alpha 2 locus, Vox Sang. 24: 481\u2013490.","journal-title":"Vox Sang"},{"key":"4_CR123","doi-asserted-by":"crossref","first-page":"1918","DOI":"10.1172\/JCI111155","volume":"72","author":"E Loghem","year":"1983","unstructured":"Van Loghem, E., Zegers, B. J. M., Bast, E. J. E., and Kater, L., 1983, Selective deficiency of immunoglobulin A2, J. Clin. Invest. 72: 1918\u20131923.","journal-title":"J. Clin. Invest"},{"key":"4_CR124","doi-asserted-by":"crossref","first-page":"10","DOI":"10.7326\/0003-4819-86-1-10","volume":"86","author":"DH Thiel","year":"1977","unstructured":"Van Thiel, D. H., Smith, W. I., Rabin, B. S., Fisher, S. E., and Lester, R. 1977, A syndrome of immunoglobulin A deficiency, diabetes mellitus, malabsorption, and a common HLA heplotype. Immunologic and genetic studies of forty-three family members, Ann. Intern. Med. 86: 10.","journal-title":"Ann. Intern. Med"},{"key":"4_CR125","first-page":"245","volume":"101","author":"CL Vassallo","year":"1970","unstructured":"Vassallo, C. L., Zawadzki, Z. A., and Simons, J. R., 1970, Recurrent respiratory infections in a family with immunoglobulin A deficiency, Am. Rev. Respir. Dis. 101: 245.","journal-title":"Am. Rev. Respir. Dis"},{"key":"4_CR126","first-page":"469","volume":"17","author":"GN Vyas","year":"1969","unstructured":"Vyas, G. N., and Fudenberg, H. H., 1969, Immunogenetic study of Am(1), the first allotype of human IgA, Clin. Res. 17: 469.","journal-title":"Clin. Res"},{"key":"4_CR127","first-page":"215","volume":"89","author":"TA Waldman","year":"1976","unstructured":"Waldman, T. A., Broder, S., Krahauer, R., et al., 1976, Defect in IgA secretion and in IgA specific suppressor cells in patients with selective IgA deficiency, Trans. Assoc. Am. Physicians 89: 215.","journal-title":"Trans. Assoc. Am. Physicians"},{"key":"4_CR128","doi-asserted-by":"crossref","first-page":"372","DOI":"10.1016\/0090-1229(81)90080-5","volume":"19","author":"RJ Warrington","year":"1981","unstructured":"Warrington, R. J., Dauder, P. J., and Rutherford, W. J., 1981, Suppression of mitogen induced human immunoglobulin (Ig)-A synthesis by heterologous antibody in IgA, Clin. Immunol. Immunopathol. 19: 372.","journal-title":"Clin. Immunol. Immunopathol"},{"key":"4_CR129","doi-asserted-by":"crossref","first-page":"698","DOI":"10.1016\/0090-1229(82)90333-6","volume":"23","author":"RS Warrington","year":"1982","unstructured":"Warrington, R. S., Rutherford, W. J., Sander, P. J., and Bees, W. C. H., 1982, Homologous antibody to human immunoglobulin (Ig)-A suppresses in vitro mitogen-induced IgA synthesis, Clin. Immunol. Immunopathol. 23: 698.","journal-title":"Clin. Immunol. Immunopathol"},{"key":"4_CR130","doi-asserted-by":"crossref","first-page":"44","DOI":"10.1016\/S0022-3476(71)80262-7","volume":"78","author":"W Wertelecki","year":"1971","unstructured":"Wertelecki, W., and Gerald, P. S., 1971, Clinical and chromosomal studies of the 18 q\u2014syndrome, J. Pediatr. 78: 44.","journal-title":"J. Pediatr"},{"key":"4_CR131","doi-asserted-by":"crossref","first-page":"155","DOI":"10.1002\/ajmg.1320030207","volume":"8","author":"MG Wilson","year":"1979","unstructured":"Wilson, M. G., Towner, J. W., Forsman, L., and Siris, E., 1979, Syndromes associated with the deletion of the long arm of chromosome 18, Am. J. Med. Genet. 8: 155\u2013174.","journal-title":"Am. J. Med. Genet"},{"key":"4_CR132","doi-asserted-by":"crossref","first-page":"333","DOI":"10.1007\/BF00430799","volume":"21","author":"AN Wilton","year":"1985","unstructured":"Wilton, A. N., Cobain, T. J., and Dawkins, R. L., 1985, Family studies of IgA deficiency, Immunogenetics 21: 333\u2013342.","journal-title":"Immunogenetics"},{"key":"4_CR133","doi-asserted-by":"crossref","first-page":"1","DOI":"10.1111\/j.0954-6820.1964.tb00640.x","volume":"176","author":"FA Wollheim","year":"1964","unstructured":"Wollheim, F. A., Belfrage, S., Coster, C., and Lindholm, H., 1964, Primary \u201cacquired\u201d hypogammaglobulinemia: Clinical and genetic aspects of nine cases, Acta Med. Scand. 176: 1.","journal-title":"Acta Med. Scand"},{"key":"4_CR134","first-page":"142","volume":"46","author":"N Yasuda","year":"1981","unstructured":"Yasuda, N. Kanoh, T., and Uchino, H., 1981, J-chain synthesis in lymphocytes from patients with selective IgA deficiency, Clin. Exp. Immunol. 46: 142\u2013148.","journal-title":"Exp. Immunol"}],"container-title":["Advances in Human Genetics"],"original-title":[],"language":"en","link":[{"URL":"http:\/\/link.springer.com\/content\/pdf\/10.1007\/978-1-4757-9065-8_4","content-type":"unspecified","content-version":"vor","intended-application":"similarity-checking"}],"deposited":{"date-parts":[[2023,7,1]],"date-time":"2023-07-01T13:35:03Z","timestamp":1688218503000},"score":1,"resource":{"primary":{"URL":"http:\/\/link.springer.com\/10.1007\/978-1-4757-9065-8_4"}},"subtitle":[],"short-title":[],"issued":{"date-parts":[[1990]]},"ISBN":["9781475790672","9781475790658"],"references-count":134,"URL":"https:\/\/doi.org\/10.1007\/978-1-4757-9065-8_4","relation":{},"subject":[],"published":{"date-parts":[[1990]]}}}