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Journal Abstract Search

135 related items for PubMed ID: 3981581

  • 1. A family with three independent autosomal translocations associated with 7q32----7qter syndrome.
    Bass HN, Sparkes RS, Lessner MM, Fox M, Phoenix B, Bernar J.
    J Med Genet; 1985 Feb; 22(1):59-63. PubMed ID: 3981581
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  • 2. A complex three way translocation resulting in two sibs with partial trisomy 3p23----3pter.
    Voss R, Gross-Kieselstein E, Hurvitz H, Dagan J, Kerem E, Zlotogora J.
    J Med Genet; 1984 Dec; 21(6):454-9. PubMed ID: 6512835
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  • 3. 'Pure' partial trisomy 2q in a male owing to malsegregation of a maternal translocation t(X;2)(p22.3;q32.1).
    Plessis G, Couturier J, Turleau C, Despoisses S, Delavenne J.
    J Med Genet; 1985 Feb; 22(1):70-3. PubMed ID: 3981584
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  • 4. Duplication-deletion with partial trisomy lq and partial monosomy 3p resulting from a maternal reciprocal translocation rcp (1;3) (q32;p25).
    Schinzel A.
    J Med Genet; 1981 Feb; 18(1):64-8. PubMed ID: 7253002
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  • 5. Partial trisomy 11,46,XX,-3,-20, + der3, + der20,t(3:11:20), resulting from a complex maternal rearrangement of chromosomes 3, 11, 20.
    Palmer CG, Poland C, Reed T, Kojetin J.
    Hum Genet; 1976 Feb 29; 31(2):219-25. PubMed ID: 1248831
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  • 6. Partial trisomy 7p in two families resulting from different balanced translocations.
    Moore CM, Pfeiffer RA, Craig-Holmes AP, Scott CI, Meisel-Stosiek M.
    Clin Genet; 1982 Feb 29; 21(2):112-21. PubMed ID: 7083611
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  • 7. Double translocation t(7;12),t(2;6) heterozygosity in one family. A contribution to the trisomy 12p syndrome.
    Bijlsma JB, de France HF, Bleeker-Wagemakers LM, Dijkstra PF.
    Hum Genet; 1978 Jan 19; 40(2):135-47. PubMed ID: 624544
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  • 11. Incomplete trisomy 22. I. Familial 11/22 translocation with 3:1 meiotic disjunction. Delineation of a common clinical picture and report of nine new cases from six families.
    Schinzel A, Schmid W, Auf der Maur P, Moser H, Degenhardt KH, Geisler M, Grubisic A.
    Hum Genet; 1981 Jan 19; 56(3):249-62. PubMed ID: 7239508
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  • 14. Two cases of trisomy 12p due to rcpt (12;21)(p11;p11) inherited through three generations.
    Parslow M, Chambers D, Drummond M, Hunter W.
    Hum Genet; 1979 Apr 05; 47(3):253-60. PubMed ID: 457115
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  • 20. Tertiary trisomy (22q11q),47,+der(22),t(11;22).
    Biederman BM, Lin CC, Lowry RB, Somerville R.
    Hum Genet; 1980 Feb 05; 53(2):173-7. PubMed ID: 7358384
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