121 related articles for article (PubMed ID: 1981473)
1. 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]
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. 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]
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. 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]
7. 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]
8. 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]
9. 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]
10. 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]
11. Comparative study of microsatellite and cytogenetic markers for detecting the origin of the nondisjoined chromosome 21 in Down syndrome.
Peterson MB; Frantzen M; Antonarakis SE; Warren AC; Van Broeckhoven C; Chakravarti A; Cox TK; Lund C; Olsen B; Poulsen H
Am J Hum Genet; 1992 Sep; 51(3):516-25. PubMed ID: 1386710
[TBL] [Abstract][Full Text] [Related]
12. A 48,XXY,+21 Down syndrome patient with additional paternal X and maternal 21.
Lorda-Sanchez I; Petersen MB; Binkert F; Maechler M; Schmid W; Adelsberger PA; Antonarakis SE; Schinzel A
Hum Genet; 1991 May; 87(1):54-6. PubMed ID: 1674717
[TBL] [Abstract][Full Text] [Related]
13. 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]
14. Studying nondisjunction of chromosome 21 with cytogenetic markers on the short arm and DNA markers encompassing the long arm.
Buraczynska M; Stewart GD; Sherman S; Freeman V; Grantham M; Uchida I; Hassold T; Kurnit DM
Prog Clin Biol Res; 1989; 311():101-13. PubMed ID: 2570424
[No Abstract] [Full Text] [Related]
15. 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]
16. Identification of chromosome 21 DNA polymorphisms for genetic studies in Alzheimer's disease and Down syndrome.
Van Camp G; Backhovens H; Cruts M; Wehnert A; Van Hul W; Stinissen P; Van Broeckhoven C
Hum Genet; 1991 Oct; 87(6):649-53. PubMed ID: 1682232
[TBL] [Abstract][Full Text] [Related]
17. Lack of evidence for association of meiotic nondisjunction with particular DNA haplotypes on chromosome 21.
Sacchi N; Gusella JF; Perroni L; Bricarelli FD; Papas TS
Proc Natl Acad Sci U S A; 1988 Jul; 85(13):4794-8. PubMed ID: 2898783
[TBL] [Abstract][Full Text] [Related]
18. Use of restriction fragment length polymorphic probes in the analysis of Down's syndrome trisomy.
Millington-Ward AM; Pearson PL
Hum Genet; 1988 Dec; 80(4):362-70. PubMed ID: 2904401
[TBL] [Abstract][Full Text] [Related]
19. Parental origin and mechanism of formation of polysomy X: an XXXXX case and four XXXXY cases determined with RFLPs.
Deng HX; Abe K; Kondo I; Tsukahara M; Inagaki H; Hamada I; Fukushima Y; Niikawa N
Hum Genet; 1991 Apr; 86(6):541-4. PubMed ID: 1673956
[TBL] [Abstract][Full Text] [Related]
20. Reduced recombination and paternal age effect in Klinefelter syndrome.
Lorda-Sanchez I; Binkert F; Maechler M; Robinson WP; Schinzel AA
Hum Genet; 1992 Jul; 89(5):524-30. PubMed ID: 1353053
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]
