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Journal Abstract Search

215 related items for PubMed ID: 7438504

  • 41. Inherited pericentric inversion of chromosome no. 2 with Robertsonian translocation (13q 14q) resulting in trisomy for chromosome 13q.
    Verma RS, Dosik H, Wexler IB.
    J Genet Hum; 1977 Dec; 25(4):295-301. PubMed ID: 599332
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  • 48. [Partial 11q trisomy due to missegregation of maternal t(11;22) (q23;q11.1) translocation (author's transl)].
    Pangalos C, Couturier J, Bartsocas C, Theodorou S.
    Nouv Presse Med; 1980 Nov 01; 9(41):3065-7. PubMed ID: 7443445
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  • 49. Mosaic 13 trisomy due to de novo 13/13 translocation with subsequent fission. Karyotype: 46,XX,-13, +t(13;13)(p11;q11)/46,XX,del(13)(p11). A second example.
    Fryns JP, Kleczkowska A, Jaeken J, Van Herck K, Van den Berghe MH.
    Ann Genet; 1989 Nov 01; 32(3):177-9. PubMed ID: 2486064
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  • 50. Proximal trisomy 13q and distal monosomy 8p in a dysmorphic and mentally retarded patient with an isodicentric chromosome 13q and a 13q/8p translocation chromosome.
    Lukusa T, van den Berghe L, Smeets E, Fryns JP.
    Ann Genet; 1999 Nov 01; 42(4):215-20. PubMed ID: 10674161
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  • 51. Two siblings with partial trisomy 15 and monosomy 21 associated with central nervous system anomalies.
    Ishida A, Sawaishi Y, Goto A, Takahashi Y, Arai H, Nakajima W, Onozaki M, Takada G.
    Tohoku J Exp Med; 1993 Dec 01; 171(4):277-83. PubMed ID: 8184402
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  • 53. [Partial trisomy for the distal part of the short arm of chromosome 11 due to paternal translocations 11/5].
    Bajolle F, Rullier J, Picard AM, Legrele G.
    Ann Genet; 1978 Sep 01; 21(3):181-5. PubMed ID: 315195
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  • 54. Alternate, adjacent 2 and 3:1 meiotic segregation products from a balanced t(13;18) (q12;q11) carrier.
    Cotton C, Cummins M, Smith A.
    Clin Genet; 1993 Oct 01; 44(4):193-5. PubMed ID: 8261649
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  • 55. 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 01; 88(4):482-3. PubMed ID: 1740326
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  • 58. Familial t(4;13) with abnormal offspring in three generations.
    Najafzadeh TM, Littman VA, Dumars KW.
    Am J Med Genet; 1983 Sep 01; 16(1):15-22. PubMed ID: 6638065
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