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Journal Abstract Search

142 related items for PubMed ID: 30240118

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  • 2. New insights into human nondisjunction of chromosome 21 in oocytes.
    Oliver TR, Feingold E, Yu K, Cheung V, Tinker S, Yadav-Shah M, Masse N, Sherman SL.
    PLoS Genet; 2008 Mar 14; 4(3):e1000033. PubMed ID: 18369452
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  • 3. The etiology of Down syndrome: Maternal MCM9 polymorphisms increase risk of reduced recombination and nondisjunction of chromosome 21 during meiosis I within oocyte.
    Pal U, Halder P, Ray A, Sarkar S, Datta S, Ghosh P, Ghosh S.
    PLoS Genet; 2021 Mar 14; 17(3):e1009462. PubMed ID: 33750944
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  • 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 14; 50(3):544-50. PubMed ID: 1347192
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  • 8. 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 14; 27(1):141-8. PubMed ID: 17546231
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  • 10. Genetic aetiology of Down syndrome birth: novel variants of maternal DNMT3B and RFC1 genes increase risk of meiosis II nondisjunction in the oocyte.
    Halder P, Pal U, Ganguly A, Ghosh P, Ray A, Sarkar S, Ghosh S.
    Mol Genet Genomics; 2023 Jan 14; 298(1):293-313. PubMed ID: 36447056
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  • 11. Association between maternal age and meiotic recombination for trisomy 21.
    Lamb NE, Yu K, Shaffer J, Feingold E, Sherman SL.
    Am J Hum Genet; 2005 Jan 14; 76(1):91-9. PubMed ID: 15551222
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  • 13. 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 14; 42(2):227-36. PubMed ID: 2893544
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  • 14. An examination of the relationship between hotspots and recombination associated with chromosome 21 nondisjunction.
    Oliver TR, Middlebrooks CD, Tinker SW, Allen EG, Bean LJ, Begum F, Feingold E, Chowdhury R, Cheung V, Sherman SL.
    PLoS One; 2014 Feb 14; 9(6):e99560. PubMed ID: 24926858
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  • 16. The association of low socioeconomic status and the risk of having a child with Down syndrome: a report from the National Down Syndrome Project.
    Hunter JE, Allen EG, Shin M, Bean LJ, Correa A, Druschel C, Hobbs CA, O'Leary LA, Romitti PA, Royle MH, Torfs CP, Freeman SB, Sherman SL.
    Genet Med; 2013 Sep 14; 15(9):698-705. PubMed ID: 23558253
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  • 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 14; 37(6):463-9. PubMed ID: 1974486
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