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4. Etiology of Down syndrome: Evidence for consistent association among altered meiotic recombination, nondisjunction, and maternal age across populations. Ghosh S, Feingold E, Dey SK. Am J Med Genet A; 2009 Jul; 149A(7):1415-20. PubMed ID: 19533770 [Abstract] [Full Text] [Related]
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11. Molecular analysis of nondisjunction in Down syndrome patients with and without atrioventricular septal defects. Zittergruen MM, Murray JC, Lauer RM, Burns TL, Sheffield VC. Circulation; 1995 Nov 15; 92(10):2803-10. PubMed ID: 7586245 [Abstract] [Full Text] [Related]
12. Down syndrome: parental origin, recombination, and maternal age. Vraneković J, Božović IB, Grubić Z, Wagner J, Pavlinić D, Dahoun S, Bena F, Culić V, Brajenović-Milić B. Genet Test Mol Biomarkers; 2012 Jan 15; 16(1):70-3. PubMed ID: 21861707 [Abstract] [Full Text] [Related]
13. New insights into human nondisjunction of chromosome 21 in oocytes. Oliver TR, Feingold E, Yu K, Cheung V, Tinker S, Yadav-Shah M, Masse N, Sherman SL. PLoS Genet; 2008 Mar 14; 4(3):e1000033. PubMed ID: 18369452 [Abstract] [Full Text] [Related]
16. To err (meiotically) is human: the genesis of human aneuploidy. Hassold T, Hunt P. Nat Rev Genet; 2001 Apr 14; 2(4):280-91. PubMed ID: 11283700 [Abstract] [Full Text] [Related]
18. Clustering of chromosomal aneuploidy and tracing of nondisjunction in man. Hansmann I. Environ Health Perspect; 1979 Aug 14; 31():23-5. PubMed ID: 159172 [Abstract] [Full Text] [Related]
20. Effect of meiotic recombination on the production of aneuploid gametes in humans. Lamb NE, Sherman SL, Hassold TJ. Cytogenet Genome Res; 2005 Aug 14; 111(3-4):250-5. PubMed ID: 16192701 [Abstract] [Full Text] [Related] Page: [Next] [New Search]