173 related articles for article (PubMed ID: 2149938)
1. 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]
2. Down syndrome due to de novo Robertsonian translocation t(14q;21q): DNA polymorphism analysis suggests that the origin of the extra 21q is maternal.
Petersen MB; Adelsberger PA; Schinzel AA; Binkert F; Hinkel GK; Antonarakis SE
Am J Hum Genet; 1991 Sep; 49(3):529-36. PubMed ID: 1831959
[TBL] [Abstract][Full Text] [Related]
3. 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]
4. Obligate short-arm exchange in de novo Robertsonian translocation formation influences placement of crossovers in chromosome 21 nondisjunction.
Berend SA; Page SL; Atkinson W; McCaskill C; Lamb NE; Sherman SL; Shaffer LG
Am J Hum Genet; 2003 Feb; 72(2):488-95. PubMed ID: 12506337
[TBL] [Abstract][Full Text] [Related]
5. 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]
6. 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]
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. 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]
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. 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. Parental origin of the extra chromosome in Down's syndrome.
Magenis RE; Overton KM; Chamberlin J; Brady T; Lovrien E
Hum Genet; 1977 Jun; 37(1):7-16. PubMed ID: 142063
[TBL] [Abstract][Full Text] [Related]
12. 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]
13. 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]
14. Molecular studies of translocations and trisomy involving chromosome 13.
Robinson WP; Bernasconi F; Dutly F; Lefort G; Romain DR; Binkert F; Schinzel AA
Am J Med Genet; 1996 Jan; 61(2):158-63. PubMed ID: 8669444
[TBL] [Abstract][Full Text] [Related]
15. Analysis of DNA polymorphisms suggests that most de novo dup(21q) chromosomes in patients with Down syndrome are isochromosomes and not translocations.
Antonarakis SE; Adelsberger PA; Petersen MB; Binkert F; Schinzel AA
Am J Hum Genet; 1990 Dec; 47(6):968-72. PubMed ID: 1978562
[TBL] [Abstract][Full Text] [Related]
16. Parental origin of the extra chromosome in Down's Syndrome.
Mikkelsen M
J Ment Defic Res; 1982 Sep; 26(Pt 3):143-51. PubMed ID: 6217343
[TBL] [Abstract][Full Text] [Related]
17. 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]
18. 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]
19. 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]
20. 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]
[Next] [New Search]
