{"status":"ok","message-type":"work","message-version":"1.0.0","message":{"indexed":{"date-parts":[[2023,11,10]],"date-time":"2023-11-10T19:34:33Z","timestamp":1699644873342},"reference-count":33,"publisher":"Springer Science and Business Media LLC","issue":"3","license":[{"start":{"date-parts":[[1978,1,1]],"date-time":"1978-01-01T00:00:00Z","timestamp":252460800000},"content-version":"tdm","delay-in-days":0,"URL":"http:\/\/www.springer.com\/tdm"}],"content-domain":{"domain":[],"crossmark-restriction":false},"short-container-title":["Hum Genet"],"published-print":{"date-parts":[[1978]]},"DOI":"10.1007\/bf00272184","type":"journal-article","created":{"date-parts":[[2004,10,4]],"date-time":"2004-10-04T12:17:03Z","timestamp":1096892223000},"page":"241-248","source":"Crossref","is-referenced-by-count":12,"title":["A fetus with recombinant of chromosome 8 inherited from her carrier father"],"prefix":"10.1007","volume":"40","author":[{"given":"Atsuko","family":"Fujimoto","sequence":"first","affiliation":[],"role":[{"role":"author","vocabulary":"crossref"}]},{"given":"Joseph W.","family":"Towner","sequence":"additional","affiliation":[],"role":[{"role":"author","vocabulary":"crossref"}]},{"given":"Susan B.","family":"Turkel","sequence":"additional","affiliation":[],"role":[{"role":"author","vocabulary":"crossref"}]},{"given":"Miriam G.","family":"Wilson","sequence":"additional","affiliation":[],"role":[{"role":"author","vocabulary":"crossref"}]}],"member":"297","reference":[{"key":"CR1","first-page":"699","volume":"27","author":"P. W. Allderdice","year":"1975","unstructured":"Allderdice, P. W., Browne, N., Murphy, D. P.: Chromosome 3 duplication q21?qter deletion p25?pter syndrome in children of carriers of pericentric inversion inv(3)(p25q21). Am. J. Hum. Genet. 27, 699?718 (1975)","journal-title":"Am. J. Hum. Genet."},{"key":"CR2","doi-asserted-by":"crossref","first-page":"302","DOI":"10.1016\/S0022-3476(74)80631-1","volume":"84","author":"L. Atkins","year":"1974","unstructured":"Atkins, L., Holmes, L. B., Riccardi, V. M.: Trisomy 8. J. Pediatr. 84, 302?304 (1974)","journal-title":"J. Pediatr."},{"key":"CR3","doi-asserted-by":"crossref","first-page":"217","DOI":"10.1007\/BF00279187","volume":"30","author":"J. Bou\ufffd","year":"1975","unstructured":"Bou\ufffd, J., Taillemite, J. L., Hazael-Massieux, P., L\ufffdonard, C., Bou\ufffd, A.: Association of pericentric inversion of chromosome 9 and reproductive failure in ten unrelated families. Humangenetik 30, 217?224 (1975)","journal-title":"Humangenetik"},{"key":"CR4","first-page":"746","volume":"26","author":"A. Chapelle de la","year":"1974","unstructured":"Chapelle, A. de la, Schr\ufffdder, J., Stenstrand, K., Fellman, J., Herva, R., Saarni, M., Anttolainen, I., Tallila, I., Tervila, L., Husa, L., Robson, E. B., Cook, P. J. L., Sanger, R.: Pericentric inversions of human chromosomes 9 and 10. Am. J. Hum. Genet. 26, 746?766 (1974)","journal-title":"Am. J. Hum. Genet."},{"key":"CR5","doi-asserted-by":"crossref","first-page":"456","DOI":"10.1016\/S0022-3476(71)80156-7","volume":"79","author":"M. M. Cohen","year":"1971","unstructured":"Cohen, M. M., Davidson, R. G.: An inherited pericentric chromosomal inversion (46,inv(3) (p-q+)) associated with skeletal anomalies. J. Pediatr. 79, 456?462 (1971)","journal-title":"J. Pediatr."},{"key":"CR6","doi-asserted-by":"crossref","first-page":"11","DOI":"10.1111\/j.1399-0004.1975.tb01948.x","volume":"8","author":"M. M. Cohen","year":"1975","unstructured":"Cohen, M. M., Rosenmann, A., Hacham-Zadeh, S., Dahan, S.: Dicentric X-isochromosome (Xqi dic) and pericentric inversion of No. 2 (inv(2)(p15q21)) in a patient with gonadal dysgenesis. Clin. Genet. 8, 11?17 (1975)","journal-title":"Clin. Genet."},{"key":"CR7","doi-asserted-by":"crossref","first-page":"307","DOI":"10.1159\/000130100","volume":"9","author":"B. F. Crandall","year":"1970","unstructured":"Crandall, B. F., Sparkes, R. S.: Pericentric inversion of a number 15 chromosome in nine members of one family. Cytogenetics 9, 307?316 (1970)","journal-title":"Cytogenetics"},{"key":"CR8","first-page":"115","volume":"17","author":"B. Dallapiccola","year":"1974","unstructured":"Dallapiccola, B., Capra, L., Preto, G., Covic, M., Dutrillaux, B.: Inversion p\ufffdricentrique du 4: inv(4)(p13q35) et trisomie du bras court du 4 par aneusomie de recombinaison. Ann. G\ufffdn\ufffdt. (Paris) 17, 115?118 (1974)","journal-title":"Ann. G\ufffdn\ufffdt. (Paris)"},{"key":"CR9","doi-asserted-by":"crossref","first-page":"245","DOI":"10.1159\/000130460","volume":"12","author":"B. Dutrillaux","year":"1973","unstructured":"Dutrillaux, B., Laurent, C., Robert, J. M., Lejeune, J.: Inversion p\ufffdricentrique, inv(10), chez la m\ufffdre et aneusomie de recombinaison, inv(10), rec(10), chez son fils. Cytogenet. Cell Genet. 12, 245?253 (1973)","journal-title":"Cytogenet. Cell Genet."},{"key":"CR10","doi-asserted-by":"crossref","first-page":"217","DOI":"10.1001\/archpedi.1974.02110270091019","volume":"128","author":"J. I. Escobar","year":"1974","unstructured":"Escobar, J. I., Sanchez, O., Yunis, J. J.: Trisomy for the distal segment of chromosome 13. Am. J. Dis. Child. 128, 217?220 (1974)","journal-title":"Am. J. Dis. Child."},{"key":"CR11","doi-asserted-by":"crossref","first-page":"400","DOI":"10.1159\/000130206","volume":"11","author":"M. J. W. Faed","year":"1972","unstructured":"Faed, M. J. W., Marrian, V. J., Robertson, J., Robson, E. B., Cook, P. J. L.: Inherited pericentric inversion of chromosome 5: A family with history of neonatal death and a case of the ?cri du chat? syndrome. Cytogenetics 11, 400?411 (1972)","journal-title":"Cytogenetics"},{"key":"CR12","doi-asserted-by":"crossref","first-page":"67","DOI":"10.1007\/BF00283508","volume":"27","author":"A. Fujimoto","year":"1975","unstructured":"Fujimoto, A., Wilson, M. G., Towner, J. W.: Familial inversion of chromosome No. 8; An affected child and a carrier fetus. Humangenetik 27, 67?73 (1975)","journal-title":"Humangenetik"},{"key":"CR13","doi-asserted-by":"crossref","first-page":"413","DOI":"10.1136\/jmg.9.4.413","volume":"9","author":"H. Hauksd\ufffdttir","year":"1972","unstructured":"Hauksd\ufffdttir, H., Halld\ufffdrsson, S., Jensson, O., Mikkelsen, M., McDermott, A.: Pericentric inversion of chromosome No. 13 in a large family leading to duplication deficiency causing congenital malformations in three individuals. J. Med. Genet. 9, 413?421 (1972)","journal-title":"J. Med. Genet."},{"key":"CR14","first-page":"208","volume":"28","author":"R. Herva","year":"1976","unstructured":"Herva, R., Chapelle, A. de la: A large pericentric inversion of human chromosome 8. Am. J. Hum. Genet. 28, 208?212 (1976)","journal-title":"Am. J. Hum. Genet."},{"key":"CR15","doi-asserted-by":"crossref","first-page":"219","DOI":"10.1111\/j.1469-1809.1968.tb00552.x","volume":"31","author":"P. A. Jacobs","year":"1967","unstructured":"Jacobs, P. A., Cruickshank, G., Faed, M. J. W., Frackiewicz, A., Robson, E. B., Harris, H., Sutherland, I.: Pericentric inversion of a group C autosome: A study of three families. Ann. Hum. Genet. 31, 219?228 (1967)","journal-title":"Ann. Hum. Genet."},{"key":"CR16","doi-asserted-by":"crossref","first-page":"50","DOI":"10.1136\/jmg.11.1.50","volume":"11","author":"P. A. Jacobs","year":"1974","unstructured":"Jacobs, P. A., Buckton, K. E., Cunningham, C., Newton, M.: An analysis of the break points of structural rearrangements in man. J. Med. Genet. 11, 50?64 (1974)","journal-title":"J. Med. Genet."},{"key":"CR17","first-page":"93","volume":"26","author":"C. S. N. Lee","year":"1974","unstructured":"Lee, C. S. N., Ying, K. L., Bowen, P.: Position of the Duffy locus on chromosome 1 in relation to breakpoints for structural rearrangements. Am. J. Hum. Genet. 26, 93?102 (1974)","journal-title":"Am. J. Hum. Genet."},{"key":"CR18","first-page":"121","volume":"28","author":"C. Leonard","year":"1975","unstructured":"Leonard, C., Hazael-Massieux, P., Bocquet, L., Larget-Piet, L., Bou\ufffd, J.: Inversion p\ufffdricentrique inv(2)(p11q13) dans des families non apparent\ufffdes. Humangenetik 28, 121?128 (1975)","journal-title":"Humangenetik"},{"key":"CR19","doi-asserted-by":"crossref","first-page":"126","DOI":"10.1159\/000130332","volume":"14","author":"A. G. J. M. Linden van der","year":"1975","unstructured":"Linden, A. G. J. M. van der, Pearson, P. L., Kamp, J. J. P. van de. Cytological assessment of meiotic exchanges in a human male with a pericentric inversion of chromosome No. 4. Cytogenet. Cell Genet. 14, 126?139 (1975)","journal-title":"Cytogenet. Cell Genet."},{"key":"CR20","doi-asserted-by":"crossref","first-page":"305","DOI":"10.1111\/j.1469-1809.1975.tb00614.x","volume":"38","author":"A. McDermott","year":"1975","unstructured":"McDermott, A., Parrington, J. M.: Elucidation of a pericentric inversion of a D-group chromosome in the mother of a child with Patau's syndrome. Ann. Hum. Genet. 38, 305?307 (1975)","journal-title":"Ann. Hum. Genet."},{"key":"CR21","doi-asserted-by":"crossref","first-page":"478","DOI":"10.1136\/jmg.9.4.478","volume":"9","author":"S. Mori?-Petrovi?","year":"1972","unstructured":"Mori?-Petrovi?, S., La?a, A., Kali?anin, P.: Down's syndrome with an atypical G\/G translocation derived from familial pericentric inversion in one chromosome of the G group. J. Med. Genet. 9, 478?484 (1972)","journal-title":"J. Med. Genet."},{"key":"CR22","doi-asserted-by":"crossref","first-page":"80","DOI":"10.1038\/newbio241080a0","volume":"241","author":"D. E. Mutton","year":"1973","unstructured":"Mutton, D. E., Daker, M. G.: Pericentric inversion of chromosome 9. Nature (New Biol.) 241, 80 (1973)","journal-title":"Nature (New Biol.)"},{"key":"CR23","doi-asserted-by":"crossref","first-page":"204","DOI":"10.1007\/BF00285214","volume":"36","author":"M. Seabright","year":"1972","unstructured":"Seabright, M.: The use of proteolytic enzymes for the mapping of structural rearrangements in the chromosomes of man. Chromosoma 36, 204?210 (1972)","journal-title":"Chromosoma"},{"key":"CR24","first-page":"343","volume":"22","author":"D. Soudek","year":"1974","unstructured":"Soudek, D., O'Shaughnessy, S., Laraya, P., McCreary, B. D.: Pericentric inversion of ?Fluorescent? segment in chromosome No. 3. Humangenetik 22, 343?346 (1974)","journal-title":"Humangenetik"},{"key":"CR25","doi-asserted-by":"crossref","first-page":"105","DOI":"10.1136\/jmg.9.1.105","volume":"9","author":"R. B. Surana","year":"1972","unstructured":"Surana, R. B., Conen, P. E.: Inherited pericentric inversion of a group D(13?15) chromosome. J. Med. Genet. 9, 105?110 (1972)","journal-title":"J. Med. Genet."},{"key":"CR26","doi-asserted-by":"crossref","first-page":"54","DOI":"10.1111\/j.1399-0004.1976.tb00009.x","volume":"10","author":"G. R. Sutherland","year":"1976","unstructured":"Sutherland, G. R., Gardiner, A. J., Carter, R. F.: Familial pericentric inversion of chromosome 19, inv(19)(p13q13) with a note on genetic counselling of pericentric inversion carriers. Clin. Genet. 10, 54?59 (1976)","journal-title":"Clin. Genet."},{"key":"CR27","doi-asserted-by":"crossref","first-page":"263","DOI":"10.1016\/S0022-3476(73)80164-7","volume":"82","author":"K. Taysi","year":"1973","unstructured":"Taysi, K., Bobrow, M., Balci, S., Madan, K., Atasu, M., Say, B.: Duplication\/deficiency product of a pericentric inversion in man: A cause of D1 trisomy syndrome. J. Pediatr. 82, 263?268 (1973)","journal-title":"J. Pediatr."},{"key":"CR28","first-page":"203","volume":"28","author":"D. T. Vine","year":"1976","unstructured":"Vine, D. T., Yarkoni, S., Cohen, M. M.: Inversion homozygosity of chromosome No. 9 in a highly inbred kindred. Am. J. Hum. Genet. 28, 203?207 (1976)","journal-title":"Am. J. Hum. Genet."},{"key":"CR29","doi-asserted-by":"crossref","first-page":"132","DOI":"10.1159\/000130182","volume":"11","author":"J. Wahrman","year":"1972","unstructured":"Wahrman, J., Atidia, J., Goitein, R., Cohen, T.: Pericentric inversions of chromosome 9 in two families. Cytogenetics 11, 132?144 (1972)","journal-title":"Cytogenetics"},{"key":"CR30","doi-asserted-by":"crossref","first-page":"355","DOI":"10.1007\/BF00273339","volume":"20","author":"S. Warter","year":"1973","unstructured":"Warter, S., Ruch, J. V., Lehmann, M.: Karyotype with chromosomal abnormality with various inherited defects in the offspring (recombination aneusomy). Humangenetik 20, 355?359 (1973)","journal-title":"Humangenetik"},{"key":"CR31","doi-asserted-by":"crossref","first-page":"53","DOI":"10.1111\/j.1469-1809.1969.tb01629.x","volume":"33","author":"L. R. Weitkamp","year":"1969","unstructured":"Weitkamp, L. R., Janzen, M. K., Guttormsen, S. A., Gershowitz, H.: Inherited pericentric inversion of chromosome number two: A linkage study. Ann. Hum. Genet. 33, 53?57 (1969)","journal-title":"Ann. Hum. Genet."},{"key":"CR32","first-page":"679","volume":"22","author":"M. G. Wilson","year":"1970","unstructured":"Wilson, M. G., Towner, J. W., Coffin, G. S., Forsman, I.: Inherited pericentric inversion of chromosome No. 4. Am. J. Hum. Genet. 22, 679?690 (1970)","journal-title":"Am. J. Hum. Genet."},{"key":"CR33","first-page":"265","volume":"19","author":"E. Zeuthen","year":"1973","unstructured":"Zeuthen, E., Nielson, J.: Pericentric Y inversion in the general population. Humangenetik 19, 265?270 (1973)","journal-title":"Humangenetik"}],"container-title":["Human Genetics"],"original-title":[],"language":"en","link":[{"URL":"http:\/\/link.springer.com\/content\/pdf\/10.1007\/BF00272184.pdf","content-type":"application\/pdf","content-version":"vor","intended-application":"text-mining"},{"URL":"http:\/\/link.springer.com\/article\/10.1007\/BF00272184\/fulltext.html","content-type":"text\/html","content-version":"vor","intended-application":"text-mining"},{"URL":"http:\/\/link.springer.com\/content\/pdf\/10.1007\/BF00272184","content-type":"unspecified","content-version":"vor","intended-application":"similarity-checking"}],"deposited":{"date-parts":[[2023,4,29]],"date-time":"2023-04-29T12:26:48Z","timestamp":1682771208000},"score":1,"resource":{"primary":{"URL":"http:\/\/link.springer.com\/10.1007\/BF00272184"}},"subtitle":[],"short-title":[],"issued":{"date-parts":[[1978]]},"references-count":33,"journal-issue":{"issue":"3","published-print":{"date-parts":[[1978]]}},"alternative-id":["BF00272184"],"URL":"https:\/\/doi.org\/10.1007\/bf00272184","relation":{},"ISSN":["0340-6717","1432-1203"],"issn-type":[{"value":"0340-6717","type":"print"},{"value":"1432-1203","type":"electronic"}],"subject":[],"published":{"date-parts":[[1978]]}}}