These tools will no longer be maintained as of December 31, 2024. Archived website can be found here. PubMed4Hh GitHub repository can be found here. Contact NLM Customer Service if you have questions.


BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

202 related articles for article (PubMed ID: 2571561)

  • 1. 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]  

  • 2. 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]  

  • 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. 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]  

  • 5. 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]  

  • 6. 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]  

  • 7. 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]  

  • 8. 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]  

  • 9. 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]  

  • 10. 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]  

  • 11. 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]  

  • 12. 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]  

  • 13. 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]  

  • 14. 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]  

  • 15. 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]  

  • 16. 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]  

  • 17. The parental origin of the missing or additional chromosome in 45,X and 47,XXX females.
    Hassold T; Arnovitz K; Jacobs PA; May K; Robinson D
    Birth Defects Orig Artic Ser; 1990; 26(4):297-304. PubMed ID: 1982521
    [TBL] [Abstract][Full Text] [Related]  

  • 18. Double aneuploidy in three Egyptian patients: Down-Turner and Down-Klinefelter syndromes.
    Zaki MS; Kamel AA; El-Ruby M
    Genet Couns; 2005; 16(4):393-402. PubMed ID: 16440882
    [TBL] [Abstract][Full Text] [Related]  

  • 19. [Down-Turner syndrome (45,X/47,XY,+21): case report and review].
    Ryu SW; Lee G; Baik CS; Shim SH; Kim JT; Lee JS; Lee KA
    Korean J Lab Med; 2010 Apr; 30(2):195-200. PubMed ID: 20445340
    [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]
    of 11.