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Pubmed for Handhelds

PUBMED FOR HANDHELDS

Journal Abstract Search

145 related items for PubMed ID: 589852

  • 61.
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  • 63. Trisomy 6p22 leads to 6pter due to familial t(6;13)(p22;q34 or 33) translocation.
    Rosi G, Venti G, Migliorini Brushelli G, Donti E, Bocchini V, Armellini R.
    Hum Genet; 1979 Sep 02; 51(1):67-72. PubMed ID: 500094
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  • 64. Five generations of t(4;8)(q35;q13) leading to a case of partial 8q trisomy with consideration of potential pregnancy outcomes from translocation carriers.
    Young RS, Hansen KL, Khodr GS.
    Clin Genet; 1984 Jun 02; 25(6):522-7. PubMed ID: 6733948
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  • 67. 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 02; 25(6):500-21. PubMed ID: 6539659
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  • 71. [Partial trisomy 1 (1q31-41) caused by intrachromosomal insertion in 1p31.3 in a newborn infant and a sister of the mother].
    Pfeiffer RA, Englisch W.
    Monatsschr Kinderheilkd; 1987 Dec 02; 135(12):851-6. PubMed ID: 3437908
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  • 72.
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  • 73. Structural aberrations of the long arm of chromosome no. 22. Report fo a family with translocation t(11;22) (q25;q11).
    Fu W, Borgaonkar DS, Ladewig PP, Weaver J, Pomerance HH.
    Clin Genet; 1976 Dec 02; 10(6):329-36. PubMed ID: 991443
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  • 76. 46, XY, t(3;22) (p2;q13) resulting in partial trisomy for the short arm of chromosome 3.
    Surana RB, Braudo ME, Conen PE, Slade RH.
    Clin Genet; 1977 Mar 02; 11(3):201-6. PubMed ID: 837571
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  • 77. Two cases of partial trisomy 10q syndrome due to a familial 10;20 translocation.
    Tüysüz B, Hacihanefioglu S, Silahtaroglu A, Yilmaz S, Deviren A, Cenani A.
    Genet Couns; 2000 Mar 02; 11(4):355-61. PubMed ID: 11140413
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