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Journal Abstract Search

199 related items for PubMed ID: 9147886

  • 1. 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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  • 2. 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 Dec; 35(4):231-3. PubMed ID: 1296521
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  • 5. 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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  • 9. Familial translocation t(10;14) (q26.1;q32.3): report of three offspring with 10q deletion and 14q duplication.
    Huang TH, Peckham D, Batanian JR, Martin MB, Kouba M, Caldwell CW, Miles JH.
    Clin Genet; 1994 Oct; 46(4):299-303. PubMed ID: 7834895
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  • 11. A paternal balanced translocation [t(7;22)(q32;q13.3)] leading to reciprocal unbalanced karyotypes in two consecutive pregnancies.
    Zackowski JL, Raffel LJ, McDaniel LD, Schwartz S.
    Ann Genet; 1990 Oct; 33(2):113-6. PubMed ID: 2241085
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  • 12. A familial "balanced" 3;9 translocation with cryptic 8q insertion leading to deletion and duplication of 9p23 loci in siblings.
    Wagstaff J, Hemann M.
    Am J Hum Genet; 1995 Jan; 56(1):302-9. PubMed ID: 7825591
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  • 13. A severely mental and motor retarded boy with monosomy 9pter-->p22 trisomy 10q26-->qter due to paternal reciprocal translocation 46,XY,t(9;10)(p23;q26).
    Akbas E, Polat S, Karakas-Celik S, Altintas ZM, Yildirim M, Yilgor E.
    Genet Couns; 2011 Jan; 22(4):417-23. PubMed ID: 22303803
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  • 16. 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. Familial Wolf's syndrome with a hidden 4p deletion by translocation of an 8p segment. Unbalanced inheritance from a maternal translocation (4;8)(p15.3;p22). Case report, review and risk estimates.
    Stengel-Rutkowski S, Warkotsch A, Schimanek P, Stene J.
    Clin Genet; 1984 Jun; 25(6):500-21. PubMed ID: 6539659
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