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Journal Abstract Search

168 related items for PubMed ID: 2793173

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  • 2. The unbalanced offspring of the male carriers of the 11q;22q translocation: nondisjunction at meiosis II in a balanced spermatocyte.
    Simi P, Ceccarelli M, Barachini A, Floridia G, Zuffardi O.
    Hum Genet; 1992 Feb; 88(4):482-3. PubMed ID: 1740326
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  • 3. Unbalanced karyotype due to adjacent 1 segregation of t(11;22)(q23.3;q13.2).
    Tachdjian G, Muti C, Gaudelus J, Druart L, Martin B, Tamboise E, Nessmann C.
    Ann Genet; 1992 Feb; 35(4):231-3. PubMed ID: 1296521
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  • 4. A unique case of der(11)t(11;22),-22 arising from 3:1 segregation of a maternal t(11;22) in a family with co-segregation of the translocation and breast cancer.
    Jobanputra V, Chung WK, Hacker AM, Emanuel BS, Warburton D.
    Prenat Diagn; 2005 Aug; 25(8):683-6. PubMed ID: 16049998
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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; 32(1):24-9. PubMed ID: 2721946
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  • 8. 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; 33(11):952-6. PubMed ID: 8950677
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  • 13. The 11q;22q translocation: a collaborative study of 20 new cases and analysis of 110 families.
    Iselius L, Lindsten J, Aurias A, Fraccaro M, Bastard C, Bottelli AM, Bui TH, Caufin D, Dalprà L, Delendi N.
    Hum Genet; 1983 Nov; 64(4):343-55. PubMed ID: 6618487
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  • 15. Multicolor fluorescence in situ hybridization analysis of the spermatozoa of a male heterozygous for a reciprocal translocation t(11;22)(q23;q11).
    Estop AM, Cieply KM, Munne S, Feingold E.
    Hum Genet; 1999 May; 104(5):412-7. PubMed ID: 10394934
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  • 16. Inheritance of imbalances in recurrent chromosomal translocation t(11;22): clarification by PGT-SR and sperm-FISH analysis.
    Zenagui R, Bernicot I, Ranisavljevic N, Haquet E, Ferrieres-Hoa A, Pellestor F, Anahory T.
    Reprod Biomed Online; 2019 Jul; 39(1):40-48. PubMed ID: 31097322
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  • 17. Predisposition for breast cancer in carriers of constitutional translocation 11q;22q.
    Lindblom A, Sandelin K, Iselius L, Dumanski J, White I, Nordenskjöld M, Larsson C.
    Am J Hum Genet; 1994 May; 54(5):871-6. PubMed ID: 8178827
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  • 18. Emanuel syndrome due to unusual segregation of paternal origin.
    Zaki MS, Mohamed AM, Kamel AK, El-Gerzawy AM, El-Ruby MO.
    Genet Couns; 2012 May; 23(2):319-28. PubMed ID: 22876593
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  • 20. A small (sSMC) chromosome 22 due to a maternal translocation between chromosomes 8 and 22: a case report.
    Mundhofir FE, Kooper AJ, Winarni TI, Smits AP, Faradz SM, Hamel BC.
    Genet Couns; 2010 May; 21(1):99-108. PubMed ID: 20420036
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