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Journal Abstract Search

106 related items for PubMed ID: 1427783

  • 1.
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  • 2. 11q;22q translocation: third case of imbalance not due to 3:1 nondisjunction in first meiosis.
    Lurie IW, Podleschuk LV.
    Am J Med Genet; 1992 Jan 15; 42(2):216. PubMed ID: 1733172
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  • 4. Not all chromosome imbalance resulting from the 11q;22q translocation is due to 3:1 segregation in first meiosis.
    Lockwood DH, Farrier A, Hecht F, Allanson J.
    Hum Genet; 1989 Oct 15; 83(3):287-8. PubMed ID: 2793173
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  • 5. Unusual segregation of t(11;22) resulting from crossing-over followed by 3:1 disjunction at meiosis I.
    Petković I, de Capoa A, Giancotti P, Barisić I.
    Clin Genet; 1996 Dec 15; 50(6):515-9. PubMed ID: 9147886
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  • 6. Second meiotic nondisjunction of the rearranged chromosome in a familial reciprocal 5/13 translocation.
    Masuno M, Cholsong Y, Kuwahara T, Shimizu N, Yamaguchi S, Kawabata I, Tamaya T, Morishita Y, Yoshimi N, Orii T.
    Am J Med Genet; 1991 Oct 01; 41(1):32-4. PubMed ID: 1951460
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  • 7. Meiotic chromosome segregation in human t(11;22)(q23;q11) carriers: a theoretical consideration.
    Koduru PR, Chaganti RS.
    Genome; 1989 Feb 01; 32(1):24-9. PubMed ID: 2721946
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  • 9. Unequal nondisjunction frequencies of trivalent chromosomes in male mice heterozygous for two Robertsonian translocations.
    Winking H, Reuter C, Bostelmann H.
    Cytogenet Cell Genet; 2000 Feb 01; 91(1-4):303-6. PubMed ID: 11173874
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  • 11. Emanuel syndrome due to unusual segregation of paternal origin.
    Zaki MS, Mohamed AM, Kamel AK, El-Gerzawy AM, El-Ruby MO.
    Genet Couns; 2012 Feb 01; 23(2):319-28. PubMed ID: 22876593
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  • 12. Is there an interchromosomal effect in reciprocal translocation carriers? Sperm FISH studies.
    Estop AM, Cieply K, Munne S, Surti U, Wakim A, Feingold E.
    Hum Genet; 2000 May 01; 106(5):517-24. PubMed ID: 10914681
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  • 13. Unusual chromosomal mosaicism as a cause of mental retardation and congenital malformations in a familial reciprocal translocation carrier, t(17;22)(q24.2;q11.23).
    Dufke A, Mayrhofer H, Enders H, Kaiser P, Leipoldt M.
    Cytogenet Cell Genet; 2001 May 01; 93(3-4):168-70. PubMed ID: 11528107
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  • 15. Der(22)t(11;22) resulting from a paternal de novo translocation, adjacent 1 segregation, and maternal heterodisomy of chromosome 22.
    Dawson AJ, Mears AJ, Chudley AE, Bech-Hansen T, McDermid H.
    J Med Genet; 1996 Nov 01; 33(11):952-6. PubMed ID: 8950677
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  • 16. Triploidy arising from a first meiotic non-disjunction in a mother carrying a reciprocal translocation.
    Rochon L, Vekemans MJ.
    J Med Genet; 1990 Nov 01; 27(11):724-6. PubMed ID: 2277393
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  • 17. [A comparison of the characteristics of chromosome nondisjunction in the first maturation division of mouse oocytes heterozygous for balanced structural rearrangements of the chromosomes].
    Chebotar' NA, Bariliak IR.
    Tsitol Genet; 1994 Nov 01; 28(2):11-9. PubMed ID: 7941016
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  • 18. The Recurrent t(11;22)(q23;q11.2) Can Occur as a Post-Zygotic Event.
    Correll-Tash S, Conlin L, Mininger BA, Lilley B, Mennuti MT, Emanuel BS.
    Cytogenet Genome Res; 2018 Nov 01; 156(4):185-190. PubMed ID: 30566958
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  • 19. Paternal origin of the de novo constitutional t(11;22)(q23;q11).
    Ohye T, Inagaki H, Kogo H, Tsutsumi M, Kato T, Tong M, Macville MV, Medne L, Zackai EH, Emanuel BS, Kurahashi H.
    Eur J Hum Genet; 2010 Jul 01; 18(7):783-7. PubMed ID: 20179746
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  • 20. Mortality and cancer incidence in carriers of constitutional t(11;22)(q23;q11) translocations: A prospective study.
    Schoemaker MJ, Jones ME, Higgins CD, Wright AF, UK Clinical Cytogenetics Group, Swerdlow AJ.
    Int J Cancer; 2019 Sep 15; 145(6):1493-1498. PubMed ID: 30496607
    [Abstract] [Full Text] [Related]

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