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The infant's derivative chromosome was apparently produced by meiotic recombination between the inversion chromosome and its normal homologue.<\/jats:p>","DOI":"10.1136\/jmg.18.1.59","type":"journal-article","created":{"date-parts":[[2008,11,10]],"date-time":"2008-11-10T14:52:06Z","timestamp":1226328726000},"page":"59-61","source":"Crossref","is-referenced-by-count":14,"title":["Trisomy 10p produced by recombination involving maternal inversion inv(10)(pllq26)."],"prefix":"10.1136","volume":"18","author":[{"given":"S C","family":"Lansky-Shafer","sequence":"first","affiliation":[],"role":[{"role":"author","vocabulary":"crossref"}]},{"given":"W L","family":"Daniel","sequence":"additional","affiliation":[],"role":[{"role":"author","vocabulary":"crossref"}]},{"given":"L","family":"Ruiz","sequence":"additional","affiliation":[],"role":[{"role":"author","vocabulary":"crossref"}]}],"member":"239","published-online":{"date-parts":[[1981,2,1]]},"reference":[{"key":"ref_1","first-page":"241","article-title":"A fetus with recombinant of chromosome","volume":"40","author":"Fujimoto, A.; Towner, J.W.; Turkel, S.B.; Wilson, M.G.","year":"1978","unstructured":"Fujimoto A, Towner JW, Turkel SB, Wilson MG. A fetus with recombinant of chromosome 8 inherited from her carrier father. Hum Genet 1978;40:241-8.","journal-title":"Hum Genet; her carrier father"},{"key":"ref_2","doi-asserted-by":"crossref","first-page":"245","DOI":"10.1159\/000130460","article-title":"Inversion pericentrique, inv(10), chez la mere et aneusomie de recombinaison, inv(10), rec(10), chez son fils","volume":"12","author":"Dutrillaux, B.; Laurent, C.; Robert, J.M.; Lejeune, J.","year":"1973","unstructured":"Dutrillaux B, Laurent C, Robert JM, Lejeune J. Inversion pericentrique, inv(10), chez la mere et aneusomie de recombinaison, inv(10), rec(10), chez son fils. Cvtogenet Cell Gentet 1973;12:245-53.","journal-title":"Cvtogenet Cell Gentet"},{"key":"ref_3","first-page":"746","article-title":"Pericentric inversions of human chromosomes 9 and 10","volume":"26","author":"de la Chapelle A; J, Schroder; K, Stenstrand","year":"1974","unstructured":"de la Chapelle A, Schroder J, Stenstrand K, et al. Pericentric inversions of human chromosomes 9 and 10. Am J Hum Genet 1974;26:746-66.","journal-title":"Am J Hum Genet"},{"key":"ref_4","doi-asserted-by":"crossref","first-page":"971","DOI":"10.1016\/S0140-6736(71)90287-X","article-title":"A rapid banding technique for human chromosomes","volume":"ii:","author":"Seabright, M.","year":"1971","unstructured":"Seabright M. A rapid banding technique for human chromosomes. Lancet 1971;ii:971-2.","journal-title":"Lancet"},{"key":"ref_5","series-title":"Proceedings 3rd Interniational Congress of Human Genetics, Chicago, 1966","first-page":"69","article-title":"Clinical cytogenetics","author":"Ferguson-Smith, M.A.","year":"1967","unstructured":"Ferguson-Smith MA. Clinical cytogenetics. In: Crow JF, Neel JV, eds. Proceedings 3rd Interniational Congress of Human Genetics, Chicago, 1966. Baltimore: Johns Hopkins Press, 1967:69-75."},{"key":"ref_6","first-page":"\"208","article-title":"A large pericentric inversion of human chromosome 8","volume":"28","author":"Herva, R.; de la Chapelle, A.","year":"1976","unstructured":"Herva R, de la Chapelle A. A large pericentric inversion of human chromosome 8. Amn J Slum Genet 1976;28: 208-12. de Grouchy J, Turleau C. Clinical atlas of human chroinosomes. New York: Wiley, 1977:100-5.","journal-title":"Amn J Slum Genet; Clinical atlas of human chroinosomes"},{"article-title":"In the series of Freidrich and Nielson,. three were found among 5029 consecutive live born children in Denmark, and Gerald and Walzer2 found an incidence of 0-8 per 1000 among 3543 newborns. In Received for publication","year":"1980","key":"ref_7","unstructured":"In the series of Freidrich and Nielson,. three were found among 5029 consecutive live born children in Denmark, and Gerald and Walzer2 found an incidence of 0-8 per 1000 among 3543 newborns. In Received for publication 15 February 1980"}],"container-title":["Journal of Medical Genetics"],"original-title":[],"language":"en","link":[{"URL":"https:\/\/syndication.highwire.org\/content\/doi\/10.1136\/jmg.18.1.59","content-type":"unspecified","content-version":"vor","intended-application":"similarity-checking"}],"deposited":{"date-parts":[[2025,10,17]],"date-time":"2025-10-17T22:26:07Z","timestamp":1760739967000},"score":1,"resource":{"primary":{"URL":"https:\/\/jmg.bmj.com\/lookup\/doi\/10.1136\/jmg.18.1.59"}},"subtitle":[],"short-title":[],"issued":{"date-parts":[[1981,2]]},"references-count":7,"journal-issue":{"issue":"1","published-online":{"date-parts":[[1981,2,1]]},"published-print":{"date-parts":[[1981,2]]}},"alternative-id":["10.1136\/jmg.18.1.59"],"URL":"https:\/\/doi.org\/10.1136\/jmg.18.1.59","relation":{},"ISSN":["0022-2593","1468-6244"],"issn-type":[{"type":"print","value":"0022-2593"},{"type":"electronic","value":"1468-6244"}],"subject":[],"published":{"date-parts":[[1981,2]]}}}