185 related articles for article (PubMed ID: 8116616)
21. 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]
22. Advanced maternal age and the risk of Down syndrome characterized by the meiotic stage of chromosomal error: a population-based study.
Yoon PW; Freeman SB; Sherman SL; Taft LF; Gu Y; Pettay D; Flanders WD; Khoury MJ; Hassold TJ
Am J Hum Genet; 1996 Mar; 58(3):628-33. PubMed ID: 8644722
[TBL] [Abstract][Full Text] [Related]
23. [Studies of meiotic origin of the extra chromosome 21 in Down syndromes detected by using (GT)n polymorphic DNA markers].
Shi QH; Zhang JX; Pan SJ; Zhang XR; Chen YF; Shan XN; Huang HJ; Yu L; Zhao SY; Zheng QP; Adler ID
Yi Chuan Xue Bao; 1998 Dec; 25(6):478-84. PubMed ID: 10465893
[TBL] [Abstract][Full Text] [Related]
24. Meiotic origin of trisomy in neoplasms: evidence in a case of erythroleukaemia.
Minelli A; Morerio C; Maserati E; Olivieri C; Panarello C; Bonvini L; Leszl A; Rosanda C; Lanino E; Danesino C; Pasquali F
Leukemia; 2001 Jun; 15(6):971-5. PubMed ID: 11417485
[TBL] [Abstract][Full Text] [Related]
25. Mosaic trisomy 13: understanding origin using SNP array.
Jinawath N; Zambrano R; Wohler E; Palmquist MK; Hoover-Fong J; Hamosh A; Batista DA
J Med Genet; 2011 May; 48(5):323-6. PubMed ID: 21097773
[TBL] [Abstract][Full Text] [Related]
26. Investigation of factors associated with paternal nondisjunction of chromosome 21.
Oliver TR; Bhise A; Feingold E; Tinker S; Masse N; Sherman SL
Am J Med Genet A; 2009 Aug; 149A(8):1685-90. PubMed ID: 19606484
[TBL] [Abstract][Full Text] [Related]
27. [The origin of an extra chromosome 21 in families of children with Down syndrome].
Davidenkova EF; Butomo IV; Kovaleva NV
Genetika; 1988 Sep; 24(9):1671-8. PubMed ID: 2974006
[TBL] [Abstract][Full Text] [Related]
28. 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]
29. Molecular study of parental origin of extra chromosome 21 in regular and de novo translocation trisomies.
Brahe C; Tassone F; Moscetti A; Millington-Ward A; Bova R; Serra A
Am J Med Genet Suppl; 1990; 7():125-8. PubMed ID: 2149938
[TBL] [Abstract][Full Text] [Related]
30. Meiotic crossing-over in nondisjoined chromosomes of children with trisomy 21 and a congenital heart defect.
Howard CM; Davies GE; Farrer MJ; Cullen LM; Coleman MM; Williamson R; Wyse RK; Palmer R; Kessling AM
Am J Hum Genet; 1993 Aug; 53(2):462-71. PubMed ID: 8101041
[TBL] [Abstract][Full Text] [Related]
31. Parental origin of the extra chromosome in trisomy 21 as indicated by analysis of DNA polymorphisms. Down Syndrome Collaborative Group.
Antonarakis SE
N Engl J Med; 1991 Mar; 324(13):872-6. PubMed ID: 1825697
[TBL] [Abstract][Full Text] [Related]
32. 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]
33. Origin and mechanism of formation of 45,X/47,XX,+21 mosaicism in a fetus.
Harada N; Abe K; Nishimura T; Sasaki K; Ishikawa M; Fujimoto M; Matsumoto T; Niikawa N
Am J Med Genet; 1998 Feb; 75(4):432-7. PubMed ID: 9482654
[TBL] [Abstract][Full Text] [Related]
34. 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]
35. Mitotic errors in chromosome 21 of human preimplantation embryos are associated with non-viability.
Katz-Jaffe MG; Trounson AO; Cram DS
Mol Hum Reprod; 2004 Feb; 10(2):143-7. PubMed ID: 14742700
[TBL] [Abstract][Full Text] [Related]
36. Parental origin of the extra chromosome in prenatally diagnosed fetal trisomy 21.
Muller F; Rebiffé M; Taillandier A; Oury JF; Mornet E
Hum Genet; 2000 Mar; 106(3):340-4. PubMed ID: 10798364
[TBL] [Abstract][Full Text] [Related]
37. Nondisjunction of human acrocentric chromosomes: studies of 432 trisomic fetuses and liveborns.
Zaragoza MV; Jacobs PA; James RS; Rogan P; Sherman S; Hassold T
Hum Genet; 1994 Oct; 94(4):411-7. PubMed ID: 7927339
[TBL] [Abstract][Full Text] [Related]
38. [Trisomy 21: fifty years between medicine and science].
Turleau C; Vekemans M
Med Sci (Paris); 2010 Mar; 26(3):267-72. PubMed ID: 20346276
[TBL] [Abstract][Full Text] [Related]
39. [Chromosome 21 mosaicism. A review].
Kovaleva NV
Tsitologiia; 2003; 45(4):434-40. PubMed ID: 14520876
[TBL] [Abstract][Full Text] [Related]
40. Chromosome 21 non-disjunction and Down syndrome birth in an Indian cohort: analysis of incidence and aetiology from family linkage data.
Ghosh S; Bhaumik P; Ghosh P; Dey SK
Genet Res (Camb); 2010 Jun; 92(3):189-97. PubMed ID: 20667163
[TBL] [Abstract][Full Text] [Related]
[Previous] [Next] [New Search]