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PUBMED FOR HANDHELDS

Journal Abstract Search


87 related items for PubMed ID: 5276956

  • 1. Mosaicism of C-chromosome (6-12), 46, XY-45, XY, C. Report of four cases.
    Sillanpää M, Salonius AL.
    Acta Paediatr Scand Suppl; 1970; 206():Suppl 206:138+. PubMed ID: 5276956
    [No Abstract] [Full Text] [Related]

  • 2. 46,XY-47,XY,C+ mosaicism in a male infant with multiple anomalies.
    Oikawa K, Kajii T, Shimba H, Sasaki M.
    Ann Genet; 1969 Jun; 12(2):102-6. PubMed ID: 5308379
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  • 3. [C-G translocation: karyotype 46, XY,t(Cq-; Gq+): parents 46, XX and 46, XY].
    Lambotte C, Carlier G, Frederic J, Keutgen J.
    Acta Paediatr Belg; 1971 Jun; 25(2):119-26. PubMed ID: 5565831
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  • 4. [Study by fluorescence of a trisomy C mosaic, probably 8: 46,XY-47,XY,?8+].
    de Grouchy J, Turleau C, Léonard C.
    Ann Genet; 1971 Mar; 14(1):69-72. PubMed ID: 5314298
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  • 9. Report of a case resembling the Proteus syndrome with a chromosome abnormality.
    Say B, Carpenter NJ.
    Am J Med Genet; 1988 Dec; 31(4):987-9. PubMed ID: 3239588
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  • 13. Partial trisomy 12p. A newborn child with karyotype 46,XY,der(11), t(11; 12) (q25; p11) mat. Case report and review.
    Ottolina de Bracamonte N, Velazco JQ, Hammond Figueroa FG.
    Acta Cient Venez; 1982 Dec; 33(4):342-7. PubMed ID: 7186725
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  • 14. Isodicentric X chromosome and mosaicism: report on two cases of 45,X/46,X,idic(Xq)/47,X,idic(Xq),idic(Xq) and review of the literature.
    Melaragno MI, Fakih LM, Cernach MC, Maccagnan P.
    Am J Med Genet; 1993 Sep 01; 47(3):357-9. PubMed ID: 8135281
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  • 18. [A new case of partial trisomy 8p].
    Gemme G, Bonioli E, Lagorio V, Bellini C, Caledoni S, Vianello MG.
    Minerva Pediatr; 1981 Dec 01; 33(24):1211-4. PubMed ID: 7038428
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