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Journal Abstract Search

171 related items for PubMed ID: 1740326

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  • 3. 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; 50(6):515-9. PubMed ID: 9147886
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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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  • 5. 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 Aug; 35(4):231-3. PubMed ID: 1296521
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  • 8. Meiotic studies of a human male carrier of the common translocation, t(11;22), suggests postzygotic selection rather than preferential 3:1 MI segregation as the cause of liveborn offspring with an unbalanced translocation.
    Armstrong SJ, Goldman AS, Speed RM, Hultén MA.
    Am J Hum Genet; 2000 Sep; 67(3):601-9. PubMed ID: 10936106
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  • 13. Prenatal diagnosis of supernumerary chromosome derivative (22) due to maternal balanced translocation in association with diaphragmatic hernia: a case report.
    Kadir RA, Hastings R, Economides DL.
    Prenat Diagn; 1997 Aug; 17(8):761-4. PubMed ID: 9267900
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  • 18. 47,XY,+der(11;22)(q23;q12) following balanced translocation t(11;22)(q23;q12)mat. Remarks on the problem of trisomy 22.
    Kessel E, Pfeiffer RA.
    Hum Genet; 1977 Jun 10; 37(1):111-6. PubMed ID: 881189
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