Monosomy 10q26-qter and trisomy 11q13-qter as a result ofde novo unbalanced translocation
Author:
Publisher
Springer Science and Business Media LLC
Subject
Genetics,General Medicine
Link
http://link.springer.com/content/pdf/10.1007/BF03195685.pdf
Reference10 articles.
1. De France HF, Beemer FA, Senders RC, Gerards LJ, Cats BP, 1984. Partial trisomy 11q due to paternal t(11q;18p); further delineation of the clinical picture. Clin Genet 25: 295–299.
2. Kogasaka R, Morohoshi T, Sawada Y, Fujiwara M, 1990. Terminal deletion of chromosome 10q and its clinical features. Acta Peadiatr Jpn 32: 83–87.
3. Maruyama K, Koizumi T, Ikeda H, 2001. Partial monosomy 10q with partial trisomy 11q due to paternal balanced translocation. J Peadiatr Child Health 37: 198–200.
4. Pihko H, Therman E, Uchida IA, 1981. Partial 11q trisomy syndrome. Hum Genet 58: 129–134.
5. Shapiro SD, Hansen KL, Pasztor LM, Diliberti JH, Jorgenson RJ, Young RS, Moore CM, 1985. Deletions of the long arm of chromosome 10. Am J Med Genet 20: 181–196.
Cited by 3 articles. 订阅此论文施引文献 订阅此论文施引文献，注册后可以免费订阅5篇论文的施引文献，订阅后可以查看论文全部施引文献
1. Clinical and molecular evaluations of siblings with “pure” 11q23.3-qter trisomy or reciprocal monosomy due to a familial translocation t (10;11) (q26;q23.3);Molecular Cytogenetics;2014-12
2. Recurrence risks for different pregnancy outcomes and meiotic segregation analysis of spermatozoa in carriers of t(1;11)(p36.22;q12.2);Journal of Human Genetics;2014-10-16
3. Combined partial trisomy 11q and partial monosomy 10p in a 19-year-old female patient: Phenotypic and genotypic findings;American Journal of Medical Genetics Part A;2011-11-03
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