{"status":"ok","message-type":"work","message-version":"1.0.0","message":{"indexed":{"date-parts":[[2024,1,15]],"date-time":"2024-01-15T10:42:24Z","timestamp":1705315344416},"reference-count":56,"publisher":"Springer Science and Business Media LLC","issue":"2","license":[{"start":{"date-parts":[[1975,6,1]],"date-time":"1975-06-01T00:00:00Z","timestamp":170812800000},"content-version":"tdm","delay-in-days":0,"URL":"https:\/\/www.springer.com\/tdm"},{"start":{"date-parts":[[1975,6,1]],"date-time":"1975-06-01T00:00:00Z","timestamp":170812800000},"content-version":"vor","delay-in-days":0,"URL":"https:\/\/www.springer.com\/tdm"}],"content-domain":{"domain":[],"crossmark-restriction":false},"short-container-title":["Hum Genet"],"published-print":{"date-parts":[[1975,6]]},"DOI":"10.1007\/bf00273324","type":"journal-article","created":{"date-parts":[[2022,5,9]],"date-time":"2022-05-09T08:04:04Z","timestamp":1652083444000},"page":"91-109","source":"Crossref","is-referenced-by-count":20,"title":["Exclusion gene mapping utilizing patients with chromosome imbalance: The HL-A system as a prototype"],"prefix":"10.1007","volume":"27","author":[{"given":"R. E.","family":"Magenis","sequence":"first","affiliation":[],"role":[{"role":"author","vocabulary":"crossref"}]},{"given":"K.","family":"Overton","sequence":"additional","affiliation":[],"role":[{"role":"author","vocabulary":"crossref"}]},{"given":"H.","family":"Wyandt","sequence":"additional","affiliation":[],"role":[{"role":"author","vocabulary":"crossref"}]},{"given":"T.","family":"Bergstrom","sequence":"additional","affiliation":[],"role":[{"role":"author","vocabulary":"crossref"}]},{"given":"F.","family":"Hecht","sequence":"additional","affiliation":[],"role":[{"role":"author","vocabulary":"crossref"}]},{"given":"E.","family":"Lovrien","sequence":"additional","affiliation":[],"role":[{"role":"author","vocabulary":"crossref"}]}],"member":"297","reference":[{"key":"BF00273324_CR1","unstructured":"Bodmer, J. G., Rocques, P., Bodmer, W. F., Colombani, J., Degas, L., Dausset, J., Piazza, A.: I. Population Studies. In: Joint Report of the Fifth International Histocompatibility Workshop, pp. 621\u2013667, 1972"},{"key":"BF00273324_CR2","doi-asserted-by":"crossref","first-page":"75","DOI":"10.1007\/BF00696016","volume":"9","author":"K. Bender","year":"1970","unstructured":"Bender, K., Burckhardt, K.: On the localization of genes on certain autosomes of man through chromosome aberrations. III. Exclusion of the possibility of gene assignment. Humangenetik 9, 75\u201385 (1970)","journal-title":"Humangenetik"},{"key":"BF00273324_CR3","first-page":"78","volume":"11","author":"K. Bender","year":"1970","unstructured":"Bender, K., Schindera, F., Kissmeyer-Nielson, F.: Localization exclusion of the HL-A genes from the short arm of human chromosome 5. Humangenetik 11, 78\u201380 (1970)","journal-title":"Humangenetik"},{"key":"BF00273324_CR4","doi-asserted-by":"crossref","unstructured":"Bootsma, D., Giblett, E. B.: Report of the committee on the genetic constitution of autosomes other than chromosome 1. In: Human gene mapping (New Haven Conference (1973) (ed. Daniel Bergsma)). Birth Defects: Original Article Series X, 21\u201328 (1974)","DOI":"10.1159\/000130227"},{"key":"BF00273324_CR5","unstructured":"Borgoankar, D. S., Bias, W. B.: HL-A loci and chromosome 6. In: Human gene mapping (New Haven Conference (1973) (ed. Daniel Bergsma)). Birth Defects: Original Article Series X, 67\u201368 (1974)"},{"key":"BF00273324_CR6","first-page":"66","volume-title":"Discussions in cytogenetics","author":"C. Burnham","year":"1962","unstructured":"Burnham, C.: Interchanges. In: Discussions in cytogenetics, pp. 66\u2013116. Minneapolis: Burgess Publ. 1962"},{"key":"BF00273324_CR7","doi-asserted-by":"crossref","first-page":"89","DOI":"10.1111\/j.1601-5223.1971.tb02363.x","volume":"67","author":"T. Caspersson","year":"1971","unstructured":"Caspersson, T., Lomakka, G., Zech, L.: The 24 fluorescence patterns of the human metaphase chromosomes-distinguishing characters and variability. Hereditas (Lund) 67, 89\u2013102 (1971)","journal-title":"Hereditas (Lund)"},{"key":"BF00273324_CR8","doi-asserted-by":"crossref","first-page":"125","DOI":"10.1111\/j.1469-1809.1969.tb01639.x","volume":"33","author":"P. J. L. Cook","year":"1969","unstructured":"Cook, P. J. L., Gray, J. E., Brack, R. A., Robson, E. B., Howlett, R. M.: Data on haptoglobin and the D group chromosomes. Ann. hum. Genet. 33, 125\u2013135 (1969)","journal-title":"Ann. hum. Genet."},{"key":"BF00273324_CR9","unstructured":"de Grouchy, J.: The 18p-, 18q- and 18r syndromes. In: Birth Defects: Original Article Series V, 74\u201387 (1969)"},{"key":"BF00273324_CR10","doi-asserted-by":"crossref","first-page":"949","DOI":"10.1073\/pnas.61.3.949","volume":"61","author":"R. P. Donahue","year":"1968","unstructured":"Donahue, R. P., Bias, W. B., Renwick, J. W., McKusick, V. A.: Probable assignment of the Duffy blood group locus to chromosome 1 in man. Proc. nat. Acad. Sci. (Wash.) 61, 949\u2013955 (1968)","journal-title":"Proc. nat. Acad. Sci. (Wash.)"},{"key":"BF00273324_CR11","first-page":"408","volume":"49","author":"T. Dobzhansky","year":"1929","unstructured":"Dobzhansky, T.: Genetical and cytological proof of translocations involving the third and fourth chromosomes of Drosophila melanogaster. Biologisches Zentralblatt 49, 408\u2013419 (1929)","journal-title":"Biologisches Zentralblatt"},{"key":"BF00273324_CR12","first-page":"745","volume-title":"Histocompatibility testing","author":"J. H. Edwards","year":"1972","unstructured":"Edwards, J. H., Allen, F. H., Glenn, K. P., Lamm, L. U., Robson, E. B.: The linkage relationships of HL-A. In: Histocompatibility testing, pp. 745\u2013751. Baltimore: Williams and Wilkins 1972"},{"key":"BF00273324_CR13","unstructured":"Fellous, M., Billardon, C., Dausset, J., Frezal, J.: Etudes de linkage enculture de cellules. II. Marqueurs antigeniques (abstract), Fourth Int. Cong. Human Genetics, Paris, pp. 66\u201367, 1971"},{"key":"BF00273324_CR14","doi-asserted-by":"crossref","first-page":"271","DOI":"10.1038\/newbio243271a0","volume":"243","author":"M. A. Furguson-Smith","year":"1973","unstructured":"Furguson-Smith, M. A., Newman, B. F., Ellis, P. M., Thomson, D. M. G.: Assignment by deletion of human red cell acid phosphatase gene locus to the short arm of chromosome 2. Nature (Lond.) New Biol. 243, 271\u2013273 (1973)","journal-title":"Nature (Lond.) New Biol."},{"key":"BF00273324_CR15","doi-asserted-by":"crossref","first-page":"378","DOI":"10.1073\/pnas.63.2.378","volume":"63","author":"J. G. Gall","year":"1969","unstructured":"Gall, J. G., Pardue, M. L.: Formation and detection of RNA-DNA hybrid molecules in cytological preparations. Proc. nat. Acad. Sci. (Wash.) 63, 378\u2013383 (1969)","journal-title":"Proc. nat. Acad. Sci. (Wash.)"},{"key":"BF00273324_CR16","doi-asserted-by":"crossref","first-page":"1261","DOI":"10.1126\/science.182.4118.1261","volume":"182","author":"J. German","year":"1973","unstructured":"German, J., Chaganti, R. S. K.: Mapping human autosomes: Assignment of the MN locus to a specific segment in the long arm of chromosome no. 2. Science 182, 1261\u20131262 (1973)","journal-title":"Science"},{"key":"BF00273324_CR17","volume-title":"Genetic markers in human blood","author":"E. Giblett","year":"1969","unstructured":"Giblett, E.: Genetic markers in human blood. Philadelphia: Davis 1969"},{"key":"BF00273324_CR18","doi-asserted-by":"crossref","unstructured":"Hamerton, J. L., Cook, P. J. L.: Report of the committee on the genetic constitution of chromosome 1. In: Human gene mapping (New Haven Conference (1973) (ed. Daniel Bergsma)). Birth Defects: Original Article Series X, 13\u201320 (1974)","DOI":"10.1159\/000130226"},{"key":"BF00273324_CR19","unstructured":"Hecht, F.: Ring-4 chromosome: Ring autosomes, lorelei of clinical-karyotype correlation and deletion mapping. Birth Defects: Original Article Series V, 106\u2013113 (1969)"},{"key":"BF00273324_CR20","first-page":"479","volume":"1","author":"K. Hirschhorn","year":"1965","unstructured":"Hirschhorn, K., Cooper, H. L., Firschein, I. L.: Deletion of short arms of chromosome 4\u20135 in a child with defects of midline fusion. Humangenetik 1, 479\u2013482 (1965)","journal-title":"Humangenetik"},{"key":"BF00273324_CR21","volume-title":"Histocompatibility testing","year":"1972","unstructured":"Histocompatibility testing (ed. J. Dausset, J. Colombani). Baltimore: Williams and Wilkins 1972"},{"key":"BF00273324_CR22","doi-asserted-by":"crossref","first-page":"268","DOI":"10.1038\/newbio233268a0","volume":"233","author":"K. W. Jones","year":"1971","unstructured":"Jones, K. W., Corneo, G.: Location of satellite and homogeneous DNA sequences on human chromosomes. Nature (Lond.) New Biol. 233, 268\u2013271 (1971)","journal-title":"Nature (Lond.) New Biol."},{"key":"BF00273324_CR23","doi-asserted-by":"crossref","first-page":"195","DOI":"10.1007\/BF00385730","volume":"20","author":"A. Jongsma","year":"1973","unstructured":"Jongsma, A., van Someren, H., Westerveld, A., Hagemeijer, A., Pearson, P.: Localization of genes on human chromosomes by studies of human-Chinese hamster somatic cell hybrids. Humangenetik 20, 195\u2013202 (1973)","journal-title":"Humangenetik"},{"key":"BF00273324_CR24","doi-asserted-by":"crossref","first-page":"1116","DOI":"10.1038\/2191116a0","volume":"219","author":"F. Kissmeyer-Nielson","year":"1968","unstructured":"Kissmeyer-Nielson, F., Svejgaard, A., Hauge, M.: Genetics of the human HL-A transplantation system. Nature (Lond.) 219, 1116\u20131119 (1968)","journal-title":"Nature (Lond.)"},{"key":"BF00273324_CR25","volume-title":"Transplantation reviews 4","author":"F. Kissmeyer-Nielson","year":"1970","unstructured":"Kissmeyer-Nielson, F., Thorsby, E.: Human transplantation antigens. In: Transplantation reviews 4 (ed. E. Moller). Baltimore: Williams and Wilkins 1970"},{"key":"BF00273324_CR26","first-page":"159","volume":"23","author":"D. Krieger","year":"1974","unstructured":"Krieger, D., Palmer, C., Beigel, A.: Human autosomal deletion mapping and HL-A. Humangenetik 23, 159\u2013160 (1974)","journal-title":"Humangenetik"},{"key":"BF00273324_CR27","doi-asserted-by":"crossref","first-page":"109","DOI":"10.1038\/newbio231109a0","volume":"231","author":"L. U. Lamm","year":"1971","unstructured":"Lamm, L. U., Svejgaard, A., Kissmeyer-Nielson, F.: PGM3: HL-A is another linkage in man. Nature (Lond.) New Biol. 231, 109\u2013110 (1971)","journal-title":"Nature (Lond.) New Biol."},{"key":"BF00273324_CR28","first-page":"79","volume":"11","author":"J. Lejeune","year":"1968","unstructured":"Lejeune, J., LaFourcade, J., Berger, R., Cruveiller, J., Rethor\u00e9, M.-O., Dutrillaux, B., Abonyi, D., J\u00e9r\u00f4me, H.: Le ph\u00e9notype (Dr). Etude de trois cas de chromosomes D en anneau. Ann. G\u00e9n\u00e9t. 11, 79\u201381 (1968)","journal-title":"Ann. G\u00e9n\u00e9t."},{"key":"BF00273324_CR29","first-page":"3098","volume":"257","author":"J. Lejeune","year":"1963","unstructured":"Lejeune, J., LaFourcade, J., Berger, R., Vialatte, J., Boeswillard, M., Serlinge, P., Turpin, R.: Trois cas de deletion partielle du bras court d'un chromosome 5. C.R. Acad. Sci. (Paris) 257, 3098\u20133102 (1963)","journal-title":"C.R. Acad. Sci. (Paris)"},{"key":"BF00273324_CR30","first-page":"265","volume":"15","author":"R. E. Magenis","year":"1972","unstructured":"Magenis, R. E., Armendares, S., Hecht, F., Weleber, R. G., Overton, K.: Identification by fluorescence of two G rings: (46,XY,21r) G deletion syndrome I and (46,XX,22r) G deletion syndrome II. Ann. G\u00e9n\u00e9t. 15, 265\u2013266 (1972)","journal-title":"Ann. G\u00e9n\u00e9t."},{"key":"BF00273324_CR31","doi-asserted-by":"crossref","first-page":"85","DOI":"10.1126\/science.170.3953.85","volume":"170","author":"R. E. Magenis","year":"1970","unstructured":"Magenis, R. E., Hecht, F., Lovrien, E. W.: Heritable fragile site on chromosome 16: Probable localization of haptoglobin locus in man. Science 170, 85\u201387 (1970)","journal-title":"Science"},{"key":"BF00273324_CR32","doi-asserted-by":"crossref","first-page":"1199","DOI":"10.1038\/2201199a0","volume":"220","author":"Y. Matsuya","year":"1968","unstructured":"Matsuya, Y., Green, H., Basilico, C.: Properties and uses of human-mouse hybrid cell lines. Nature (Lond.) 220, 1199\u20131202 (1968)","journal-title":"Nature (Lond.)"},{"key":"BF00273324_CR33","doi-asserted-by":"crossref","first-page":"613","DOI":"10.1016\/0014-4827(60)90138-5","volume":"20","author":"P. S. Moorhead","year":"1960","unstructured":"Moorhead, P. S., Nowell, P. C., Mellman, W. J., Battips, D. M., Hungerford, D. A.: Chromosome preparations of leukocytes cultured from human peripheral blood. Exp. Cell Res. 20, 613\u2013616 (1960)","journal-title":"Exp. Cell Res."},{"key":"BF00273324_CR34","first-page":"157","volume":"16","author":"E. Niebuhr","year":"1973","unstructured":"Niebuhr, E., Ottosen, J.: Ring chromosome D (13) associated with multiple congenital malformations. Ann. G\u00e9n\u00e9t. 16, 157\u2013166 (1973)","journal-title":"Ann. G\u00e9n\u00e9t."},{"key":"BF00273324_CR35","doi-asserted-by":"crossref","first-page":"193","DOI":"10.1007\/BF00284862","volume":"20","author":"S. Nyulassy","year":"1973","unstructured":"Nyulassy, S., Izakovic, V.: A comment to the Paper: Localization exclusion of the HL-A genes from the short arm of human chromosomes (Humangenetik 11, 78\u201380 (1970)). Humangenetik 20, 193\u2013194 (1973)","journal-title":"Humangenetik"},{"key":"BF00273324_CR36","series-title":"Birth Defects: Original Article Series","volume-title":"Standardization in human cytogenetics","author":"Paris Conference","year":"1972","unstructured":"Paris Conference (1971): Standardization in human cytogenetics. Birth Defects: Original Article Series, VIII. New York: The National Foundation 1972"},{"key":"BF00273324_CR37","volume-title":"Blood groups in man","author":"R. R. Race","year":"1962","unstructured":"Race, R. R., Sanger, R.: Blood groups in man, 4th Ed. Oxford: Blackwell 1962","edition":"4th Ed."},{"key":"BF00273324_CR38","doi-asserted-by":"crossref","first-page":"65","DOI":"10.1093\/oxfordjournals.bmb.a070673","volume":"25","author":"J. H. Renwick","year":"1969","unstructured":"Renwick, J. H.: Progress in mapping human autosomes. Brit. med. Bull. 25, 65\u201373 (1969)","journal-title":"Brit. med. Bull."},{"key":"BF00273324_CR39","doi-asserted-by":"crossref","first-page":"81","DOI":"10.1146\/annurev.ge.05.120171.000501","volume":"5","author":"J. H. Renwick","year":"1971","unstructured":"Renwick, J. H.: The mapping of human chromosomes. Ann. Rev. Genet. 5, 81\u2013120 (1971)","journal-title":"Ann. Rev. Genet."},{"key":"BF00273324_CR40","doi-asserted-by":"crossref","first-page":"1163","DOI":"10.1038\/2231163a0","volume":"223","author":"E. B. Robson","year":"1969","unstructured":"Robson, E. B., Polani, P. E., Dart, S. J., Jacobs, P. A., Renwick, J. H.: Probable assignment of the alpha locus of haptoglobin to chromosome 16 in man. Nature (Lond.) 223, 1163\u20131165 (1969)","journal-title":"Nature (Lond.)"},{"key":"BF00273324_CR41","unstructured":"Ruddle, F. H.: Summary of human gene map. In: Human gene mapping (New Haven Conference (1973) (ed. Daniel Bergsma)). Birth Defects: Original Article Series X, 11\u201312 (1974)"},{"key":"BF00273324_CR42","doi-asserted-by":"crossref","first-page":"69","DOI":"10.1038\/newbio232069a0","volume":"232","author":"F. H. Ruddle","year":"1971","unstructured":"Ruddle, F. H., Chapman, W. M., Ricciuti, F., Murnane, M., Klebe, R., Meera Kahn, P.: Linkage relationships of seventeen human gene loci as determined by man-mouse somatic cell hybrids. Nature (Lond.) New Biol. 232, 69\u201373 (1971)","journal-title":"Nature (Lond.) New Biol."},{"key":"BF00273324_CR43","doi-asserted-by":"crossref","unstructured":"Seabright, M.: A rapid banding technique for human chromosomes. Lancet 1971 II, 971\u2013972","DOI":"10.1016\/S0140-6736(71)90287-X"},{"key":"BF00273324_CR44","unstructured":"Shows, T. B., Bias, W. B.: Report of the committee on genetic markers; Gene markers for mapping the human genome. In: Human gene mapping (New Haven Conference (1973) (ed. Daniel Bergsma)). Birth Defects: Original Article Series X, 35\u201348 (1974)"},{"key":"BF00273324_CR45","doi-asserted-by":"crossref","first-page":"419","DOI":"10.1159\/000129917","volume":"5","author":"M. W. Steele","year":"1966","unstructured":"Steele, M. W., Breg, W. R., Eidelman, A. I., Lion, D. T., Terzakis, T. A.: A B-group ring chromosome with mosaicism in a newborn with Cri du Chat Syndrome. Cytogenetics 5, 419\u2013429 (1966)","journal-title":"Cytogenetics"},{"key":"BF00273324_CR46","doi-asserted-by":"crossref","first-page":"78","DOI":"10.1111\/j.1469-8749.1967.tb02213.x","volume":"9","author":"A. I. Taylor","year":"1967","unstructured":"Taylor, A. I.: Patau's, Edwards' and Cri du Chat syndromes: A tabulated summary of current findings. Develop. Med. Child. Neurol. 9, 78\u201386 (1967)","journal-title":"Develop. Med. Child. Neurol."},{"key":"BF00273324_CR47","first-page":"50","volume-title":"Manual of tissue typing techniques","author":"P. Terasaki","year":"1972","unstructured":"Terasaki, P.: Manual of tissue typing techniques (ed. J. G. Ray, R. C. Scott, D. B. Hare, C. E. Harris, D. E. Kayhoe), pp. 50\u201355. Bethesda, Md.: Transplantation and Immunology Branch Collaborative Research, National Institute of Allergy and Infectious Diseases, N.I.H. 1972"},{"key":"BF00273324_CR48","first-page":"655","volume-title":"Histocompatibility testing","author":"E. Thorsby","year":"1970","unstructured":"Thorsby, E., Bratlie, A.: A rapid method for preparation of pure lymphocyte suspensions. In: Histocompatibility testing (ed. P. I. Terasaki), pp. 655\u2013656. Baltimore: Williams and Wilkins 1970"},{"key":"BF00273324_CR49","doi-asserted-by":"crossref","unstructured":"Tischfield, J. A., Creagan, R. P., Nichols, E., Ruddle, F. H.: Assignment to human chromosome 20 of the gene for the isozyme of adenosine deaminase deficient in patients with combined immuno-deficiency syndrome. Abstract: American Society of Human Genetics meeting, Atlanta, Georgia, Oct. 24\u201327, 1973","DOI":"10.1159\/000152631"},{"key":"BF00273324_CR50","doi-asserted-by":"crossref","first-page":"962","DOI":"10.1073\/pnas.71.3.962","volume":"71","author":"H. Van Someren","year":"1974","unstructured":"Van Someren, H., Westerveld, A., Hagemeijer, A., Mees, J. R., Meera Khan, P., Zaalberg, O. B.: Human antigen and enzyme markers in man-Chinese hamster somatic cell hybrids: Evidence for snyteny between the HL-A, PGM3, ME1, and IPO-B loci. Proc. nat. Acad. Sci. (Wash.) 71, 962\u2013965 (1974)","journal-title":"Proc. nat. Acad. Sci. (Wash.)"},{"key":"BF00273324_CR51","doi-asserted-by":"crossref","first-page":"658","DOI":"10.1016\/S0022-3476(70)80209-8","volume":"77","author":"R. J. Warren","year":"1970","unstructured":"Warren, R. J., Rimoin, D. L.: The G-deletion syndromes. J. Pediat. 77, 658\u2013663 (1970)","journal-title":"J. Pediat."},{"key":"BF00273324_CR52","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\u201359 (1969)","journal-title":"Ann. hum. Genet."},{"key":"BF00273324_CR53","first-page":"489","volume":"115","author":"R. G. Weleber","year":"1968","unstructured":"Weleber, R. G., Hecht, F., Giblett, E.: Ring-G chromosome, a new G-deletion syndrome? Amer. J. Dis. Child. 115, 489\u2013493 (1968)","journal-title":"Amer. J. Dis. Child."},{"key":"BF00273324_CR54","doi-asserted-by":"crossref","first-page":"397","DOI":"10.1007\/BF00395654","volume":"1","author":"U. Wolf","year":"1965","unstructured":"Wolf, U., Reinwein, H., Prosch, R., Schr\u00f6ter, R., Baitsch, H.: Defizienz an den kurzen Armen eines Chromosoms Nr. 4. Humangenetik 1, 397\u2013413 (1965)","journal-title":"Humangenetik"},{"key":"BF00273324_CR55","first-page":"119","volume":"23","author":"H. E. Wyandt","year":"1974","unstructured":"Wyandt, H. E., Vlietinck, R. F., Magenis, R. E., Hecht, F.: Colored reverse banding of human chromosomes with acridine orange following alkaline\/formalin treatment: Densitometric validation and applications. Humangenetik 23, 119\u2013130 (1974)","journal-title":"Humangenetik"},{"key":"BF00273324_CR56","doi-asserted-by":"crossref","first-page":"575","DOI":"10.1139\/g68-076","volume":"10","author":"K.-L. Ying","year":"1968","unstructured":"Ying, K.-L., Ives, E.: Asymmetry of chromosome number 1 pair in three generations of a phenotypically normal family. Canad. J. Genet. Cytol. 10, 575\u2013589 (1968)","journal-title":"Canad. J. Genet. Cytol."}],"container-title":["Humangenetik"],"original-title":[],"language":"en","link":[{"URL":"https:\/\/link.springer.com\/content\/pdf\/10.1007\/BF00273324.pdf","content-type":"application\/pdf","content-version":"vor","intended-application":"text-mining"},{"URL":"https:\/\/link.springer.com\/article\/10.1007\/BF00273324\/fulltext.html","content-type":"text\/html","content-version":"vor","intended-application":"text-mining"},{"URL":"https:\/\/link.springer.com\/content\/pdf\/10.1007\/BF00273324.pdf","content-type":"application\/pdf","content-version":"vor","intended-application":"similarity-checking"}],"deposited":{"date-parts":[[2022,5,9]],"date-time":"2022-05-09T08:04:40Z","timestamp":1652083480000},"score":1,"resource":{"primary":{"URL":"https:\/\/link.springer.com\/10.1007\/BF00273324"}},"subtitle":[],"short-title":[],"issued":{"date-parts":[[1975,6]]},"references-count":56,"journal-issue":{"issue":"2","published-print":{"date-parts":[[1975,6]]}},"alternative-id":["BF00273324"],"URL":"https:\/\/doi.org\/10.1007\/bf00273324","relation":{},"ISSN":["0018-7348"],"issn-type":[{"value":"0018-7348","type":"print"}],"subject":[],"published":{"date-parts":[[1975,6]]}}}