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.


Pubmed for Handhelds

PUBMED FOR HANDHELDS

Journal Abstract Search

142 related items for PubMed ID: 30240118

  • 21.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 22. Characterization of susceptible chiasma configurations that increase the risk for maternal nondisjunction of chromosome 21.
    Lamb NE, Feingold E, Savage A, Avramopoulos D, Freeman S, Gu Y, Hallberg A, Hersey J, Karadima G, Pettay D, Saker D, Shen J, Taft L, Mikkelsen M, Petersen MB, Hassold T, Sherman SL.
    Hum Mol Genet; 1997 Sep; 6(9):1391-9. PubMed ID: 9285774
    [Abstract] [Full Text] [Related]

  • 23.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 24. The association between maternal occupation and down syndrome: A report from the national Down syndrome project.
    Keen C, Hunter JE, Allen EG, Rocheleau C, Waters M, Sherman SL.
    Int J Hyg Environ Health; 2020 Jan; 223(1):207-213. PubMed ID: 31519426
    [Abstract] [Full Text] [Related]

  • 25. 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]

  • 26. 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
    [Abstract] [Full Text] [Related]

  • 27. Trisomy of human chromosome 18: molecular studies on parental origin and cell stage of nondisjunction.
    Eggermann T, Nöthen MM, Eiben B, Hofmann D, Hinkel K, Fimmers R, Schwanitz G.
    Hum Genet; 1996 Feb; 97(2):218-23. PubMed ID: 8566957
    [Abstract] [Full Text] [Related]

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

  • 29. Detection of parental origin and cell stage errors of a double nondisjunction in a fetus by QF-PCR.
    Guzel AI, Demirhan O, Pazarbasi A, Ozgunen FT, Kocaturk-Sel S, Tastemir D.
    Genet Test Mol Biomarkers; 2009 Feb; 13(1):73-7. PubMed ID: 19309277
    [Abstract] [Full Text] [Related]

  • 30. Evidence for reduced recombination on the nondisjoined chromosomes 21 in Down syndrome.
    Warren AC, Chakravarti A, Wong C, Slaugenhaupt SA, Halloran SL, Watkins PC, Metaxotou C, Antonarakis SE.
    Science; 1987 Aug 07; 237(4815):652-4. PubMed ID: 2955519
    [Abstract] [Full Text] [Related]

  • 31. 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 Aug 07; 311():101-13. PubMed ID: 2570424
    [No Abstract] [Full Text] [Related]

  • 32. Understanding etiology of chromosome 21 nondisjunction from gene × environment models.
    Halder P, Pal U, Ganguly A, Ghosh P, Ray A, Sarkar S, Ghosh S.
    Sci Rep; 2021 Nov 17; 11(1):22390. PubMed ID: 34789805
    [Abstract] [Full Text] [Related]

  • 33. Origin and mechanisms of non-disjunction in human autosomal trisomies.
    Nicolaidis P, Petersen MB.
    Hum Reprod; 1998 Feb 17; 13(2):313-9. PubMed ID: 9557829
    [Abstract] [Full Text] [Related]

  • 34. A candidate gene analysis and GWAS for genes associated with maternal nondisjunction of chromosome 21.
    Chernus JM, Allen EG, Zeng Z, Hoffman ER, Hassold TJ, Feingold E, Sherman SL.
    PLoS Genet; 2019 Dec 17; 15(12):e1008414. PubMed ID: 31830031
    [Abstract] [Full Text] [Related]

  • 35. Correction of the evaluation of recombination in meiosis I and II nondisjunction in trisomy 21.
    Sherman S.
    Am J Hum Genet; 1992 May 17; 50(5):1137-8. PubMed ID: 1533301
    [No Abstract] [Full Text] [Related]

  • 36. Preconception folic acid supplementation and risk for chromosome 21 nondisjunction: a report from the National Down Syndrome Project.
    Hollis ND, Allen EG, Oliver TR, Tinker SW, Druschel C, Hobbs CA, O'Leary LA, Romitti PA, Royle MH, Torfs CP, Freeman SB, Sherman SL, Bean LJ.
    Am J Med Genet A; 2013 Mar 17; 161A(3):438-44. PubMed ID: 23401135
    [Abstract] [Full Text] [Related]

  • 37. Epidemiology of Down syndrome: new insight into the multidimensional interactions among genetic and environmental risk factors in the oocyte.
    Ghosh S, Hong CS, Feingold E, Ghosh P, Ghosh P, Bhaumik P, Dey SK.
    Am J Epidemiol; 2011 Nov 01; 174(9):1009-16. PubMed ID: 21957181
    [Abstract] [Full Text] [Related]

  • 38. Paternal nondisjunction in trisomy 21: excess of male patients.
    Petersen MB, Antonarakis SE, Hassold TJ, Freeman SB, Sherman SL, Avramopoulos D, Mikkelsen M.
    Hum Mol Genet; 1993 Oct 01; 2(10):1691-5. PubMed ID: 8268923
    [Abstract] [Full Text] [Related]

  • 39. Maternal age and risk for trisomy 21 assessed by the origin of chromosome nondisjunction: a report from the Atlanta and National Down Syndrome Projects.
    Allen EG, Freeman SB, Druschel C, Hobbs CA, O'Leary LA, Romitti PA, Royle MH, Torfs CP, Sherman SL.
    Hum Genet; 2009 Feb 01; 125(1):41-52. PubMed ID: 19050929
    [Abstract] [Full Text] [Related]

  • 40. 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 Feb 01; 42(1):11-5. PubMed ID: 10214502
    [Abstract] [Full Text] [Related]

    Page: [Previous] [Next] [New Search]
    of 8.