183 related articles for article (PubMed ID: 1981472)
1. Origin of extra chromosome 21 in 343 families: cytogenetic and molecular approaches.
Dagna Bricarelli F; Pierluigi M; Grasso M; Strigini P; Perroni L
Am J Med Genet Suppl; 1990; 7():129-32. PubMed ID: 1981472
[TBL] [Abstract][Full Text] [Related]
2. 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]
3. High efficiency in the attribution of parental origin of non-disjunction in trisomy 21 by both cytogenetic and molecular polymorphisms.
Bricarelli FD; Pierluigi M; Perroni L; Grasso M; Arslanian A; Sacchi N
Hum Genet; 1988 Jun; 79(2):124-7. PubMed ID: 2899052
[TBL] [Abstract][Full Text] [Related]
4. 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]
5. Nondisjunction of chromosome 21.
Takaesu N; Jacobs PA; Cockwell A; Blackston RD; Freeman S; Nuccio J; Kurnit DM; Uchida I; Freeman V; Hassold T
Am J Med Genet Suppl; 1990; 7():175-81. PubMed ID: 1981476
[TBL] [Abstract][Full Text] [Related]
6. Nondisjunction of chromosome 21: comparisons of cytogenetic and molecular studies of the meiotic stage and parent of origin.
Lorber BJ; Grantham M; Peters J; Willard HF; Hassold TJ
Am J Hum Genet; 1992 Dec; 51(6):1265-76. PubMed ID: 1463010
[TBL] [Abstract][Full Text] [Related]
7. 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]
8. Study of the origin of nondisjunction in a family with two cases of Down syndrome using cytogenetic and molecular polymorphisms.
Stinissen P; Van Roy B; Van Camp G; Backhovens H; Partoens P; Wehnert A; Verniers H; Dumon J; Vandenberghe A; Van Broeckhoven C
Am J Med Genet Suppl; 1990; 7():133-6. PubMed ID: 1981473
[TBL] [Abstract][Full Text] [Related]
9. Parental origin of autosomal trisomies.
Hassold T; Chiu D; Yamane JA
Ann Hum Genet; 1984 May; 48(2):129-44. PubMed ID: 6234852
[TBL] [Abstract][Full Text] [Related]
10. Crossing over and chromosome 21 nondisjunction: a study of 60 families.
Perroni L; Dagna Bricarelli F; Grasso M; Pierluigi M; Baldi M; Pedemonte C; Strigini P
Am J Med Genet Suppl; 1990; 7():141-7. PubMed ID: 1981474
[TBL] [Abstract][Full Text] [Related]
11. 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]
12. 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]
13. 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]
14. Isolation of chromosome-21-specific DNA probes and their use in the analysis of nondisjunction in Down syndrome.
Galt J; Boyd E; Connor JM; Ferguson-Smith MA
Hum Genet; 1989 Jan; 81(2):113-9. PubMed ID: 2563248
[TBL] [Abstract][Full Text] [Related]
15. Distribution of meiotic recombination along nondisjunction chromosomes 21 in Down syndrome determined using cytogenetics and RFLP haplotyping.
Meijer H; Hamers GJ; Jongbloed RJ; Vaes-Peeters GP; van der Hulst RR; Geraedts JP
Hum Genet; 1989 Oct; 83(3):280-6. PubMed ID: 2571564
[TBL] [Abstract][Full Text] [Related]
16. 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]
17. Parental age and the origin of extra chromosome 21 in Down syndrome.
Jyothy A; Kumar KS; Mallikarjuna GN; Babu Rao V; Uma Devi B; Sujatha M; Reddy PP
J Hum Genet; 2001; 46(6):347-50. PubMed ID: 11393539
[TBL] [Abstract][Full Text] [Related]
18. Recurrent trisomy 21 in a couple with a child presenting trisomy 21 mosaicism and maternal uniparental disomy for chromosome 21 in the euploid cell line.
Bruyère H; Rupps R; Kuchinka BD; Friedman JM; Robinson WP
Am J Med Genet; 2000 Sep; 94(1):35-41. PubMed ID: 10982480
[TBL] [Abstract][Full Text] [Related]
19. 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]
20. Rate of recombination of chromosomes 21 in parents of children with Down syndrome.
Hamers AJ; Meyer H; Jongbloed RJ; van der Hulst RR; Geraedts JP
Clin Genet; 1990 Jun; 37(6):463-9. PubMed ID: 1974486
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]
