358 related articles for article (PubMed ID: 11173856)
1. Nondisjunction in trisomy 21: origin and mechanisms.
Petersen MB; Mikkelsen M
Cytogenet Cell Genet; 2000; 91(1-4):199-203. PubMed ID: 11173856
[TBL] [Abstract][Full Text] [Related]
2. Origin and mechanisms of non-disjunction in human autosomal trisomies.
Nicolaidis P; Petersen MB
Hum Reprod; 1998 Feb; 13(2):313-9. PubMed ID: 9557829
[TBL] [Abstract][Full Text] [Related]
3. The meiotic stage of nondisjunction in trisomy 21: determination by using DNA polymorphisms.
Antonarakis SE; Petersen MB; McInnis MG; Adelsberger PA; Schinzel AA; Binkert F; Pangalos C; Raoul O; Slaugenhaupt SA; Hafez M
Am J Hum Genet; 1992 Mar; 50(3):544-50. PubMed ID: 1347192
[TBL] [Abstract][Full Text] [Related]
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
[TBL] [Abstract][Full Text] [Related]
5. Trisomy 21 (Down syndrome): studying nondisjunction and meiotic recombination by using cytogenetic and molecular polymorphisms that span chromosome 21.
Stewart GD; Hassold TJ; Berg A; Watkins P; Tanzi R; Kurnit DM
Am J Hum Genet; 1988 Feb; 42(2):227-36. PubMed ID: 2893544
[TBL] [Abstract][Full Text] [Related]
6. Paternal nondisjunction in trisomy 21: excess of male patients.
Petersen MB; Antonarakis SE; Hassold TJ; Freeman SB; Sherman SL; Avramopoulos D; Mikkelsen M
Hum Mol Genet; 1993 Oct; 2(10):1691-5. PubMed ID: 8268923
[TBL] [Abstract][Full Text] [Related]
7. Risk of Down syndrome birth: Consanguineous marriage is associated with maternal meiosis-II nondisjunction at younger age and without any detectable recombination error.
Ray A; Oliver TR; Halder P; Pal U; Sarkar S; Dutta S; Ghosh S
Am J Med Genet A; 2018 Nov; 176(11):2342-2349. PubMed ID: 30240118
[TBL] [Abstract][Full Text] [Related]
8. Parental origin and meiotic stage of non-disjunction in 139 cases of trisomy 21.
Ballesta F; Queralt R; Gómez D; Solsona E; Guitart M; Ezquerra M; Moreno J; Oliva R
Ann Genet; 1999; 42(1):11-5. PubMed ID: 10214502
[TBL] [Abstract][Full Text] [Related]
9. Parental origin, nondisjunction, and recombination of the extra chromosome 21 in Down syndrome: a study in a sample of the Colombian population.
Ramírez NJ; Belalcázar HM; Yunis JJ; Quintero LN; Arboleda GH; Arboleda H
Biomedica; 2007 Mar; 27(1):141-8. PubMed ID: 17546231
[TBL] [Abstract][Full Text] [Related]
10. Susceptible chiasmate configurations of chromosome 21 predispose to non-disjunction in both maternal meiosis I and meiosis II.
Lamb NE; Freeman SB; Savage-Austin A; Pettay D; Taft L; Hersey J; Gu Y; Shen J; Saker D; May KM; Avramopoulos D; Petersen MB; Hallberg A; Mikkelsen M; Hassold TJ; Sherman SL
Nat Genet; 1996 Dec; 14(4):400-5. PubMed ID: 8944019
[TBL] [Abstract][Full Text] [Related]
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; 92(10):2803-10. PubMed ID: 7586245
[TBL] [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; 16(1):70-3. PubMed ID: 21861707
[TBL] [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; 4(3):e1000033. PubMed ID: 18369452
[TBL] [Abstract][Full Text] [Related]
14. Association between maternal age and meiotic recombination for trisomy 21.
Lamb NE; Yu K; Shaffer J; Feingold E; Sherman SL
Am J Hum Genet; 2005 Jan; 76(1):91-9. PubMed ID: 15551222
[TBL] [Abstract][Full Text] [Related]
15. Recombination and maternal age-dependent nondisjunction: molecular studies of trisomy 16.
Hassold T; Merrill M; Adkins K; Freeman S; Sherman S
Am J Hum Genet; 1995 Oct; 57(4):867-74. PubMed ID: 7573048
[TBL] [Abstract][Full Text] [Related]
16. To err (meiotically) is human: the genesis of human aneuploidy.
Hassold T; Hunt P
Nat Rev Genet; 2001 Apr; 2(4):280-91. PubMed ID: 11283700
[TBL] [Abstract][Full Text] [Related]
17. Coincident maternal meiotic nondisjunction of chromosomes X and 21 without evidence of autosomal asynapsis.
Ikonen RS; Lindlöf M; Janas MO; Simola KO; Millington-Ward A; de la Chapelle A
Hum Genet; 1989 Oct; 83(3):235-8. PubMed ID: 2571561
[TBL] [Abstract][Full Text] [Related]
18. Clustering of chromosomal aneuploidy and tracing of nondisjunction in man.
Hansmann I
Environ Health Perspect; 1979 Aug; 31():23-5. PubMed ID: 159172
[TBL] [Abstract][Full Text] [Related]
19. Trisomy 21: association between reduced recombination and nondisjunction.
Sherman SL; Takaesu N; Freeman SB; Grantham M; Phillips C; Blackston RD; Jacobs PA; Cockwell AE; Freeman V; Uchida I
Am J Hum Genet; 1991 Sep; 49(3):608-20. PubMed ID: 1831960
[TBL] [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; 111(3-4):250-5. PubMed ID: 16192701
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]