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Journal Abstract Search

152 related items for PubMed ID: 1974486

  • 1. 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
    [Abstract] [Full Text] [Related]

  • 2. 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 Jun; 7():175-81. PubMed ID: 1981476
    [Abstract] [Full Text] [Related]

  • 3. 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
    [Abstract] [Full Text] [Related]

  • 4. 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 Mar; 7():141-7. PubMed ID: 1981474
    [Abstract] [Full Text] [Related]

  • 5. 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
    [Abstract] [Full Text] [Related]

  • 6. 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
    [Abstract] [Full Text] [Related]

  • 7. 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
    [Abstract] [Full Text] [Related]

  • 8. Risk of Down syndrome birth: Consanguineous marriage is associated with maternal meiosis-II nondisjunction at younger age and without any detectable recombination error.
    Ray A, Oliver TR, Halder P, Pal U, Sarkar S, Dutta S, Ghosh S.
    Am J Med Genet A; 2018 Nov; 176(11):2342-2349. PubMed ID: 30240118
    [Abstract] [Full Text] [Related]

  • 9. Nondisjunction in trisomy 21: origin and mechanisms.
    Petersen MB, Mikkelsen M.
    Cytogenet Cell Genet; 2000 Nov; 91(1-4):199-203. PubMed ID: 11173856
    [Abstract] [Full Text] [Related]

  • 10. 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 Nov; 42(1):11-5. PubMed ID: 10214502
    [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
    [Abstract] [Full Text] [Related]

  • 12. 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 Oct; 7():125-8. PubMed ID: 2149938
    [Abstract] [Full Text] [Related]

  • 13. 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 Oct; 7():129-32. PubMed ID: 1981472
    [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 15; 92(10):2803-10. PubMed ID: 7586245
    [Abstract] [Full Text] [Related]

  • 15. 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 15; 87(1):54-6. PubMed ID: 1674717
    [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 May 15; 311():101-13. PubMed ID: 2570424
    [No Abstract] [Full Text] [Related]

  • 17. Parental origin of chromosomes in Down's syndrome.
    Manning CH, Goodman HO.
    Hum Genet; 1981 May 15; 59(2):101-3. PubMed ID: 6459985
    [Abstract] [Full Text] [Related]

  • 18. 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 May 15; 46(6):347-50. PubMed ID: 11393539
    [Abstract] [Full Text] [Related]

  • 19. [The parental origin of the extra chromosome 21 in Down's syndrome].
    Hamers AJ, Heijnen GC, Jongbloet PH.
    Tijdschr Kindergeneeskd; 1983 Oct 15; 51(5):157-62. PubMed ID: 6230758
    [Abstract] [Full Text] [Related]

  • 20. [The origin of an extra chromosome 21 in families of children with Down syndrome].
    Davidenkova EF, Butomo IV, Kovaleva NV.
    Genetika; 1988 Sep 15; 24(9):1671-8. PubMed ID: 2974006
    [Abstract] [Full Text] [Related]

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