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Journal Abstract Search

87 related items for PubMed ID: 5276956

  • 21. [Partial trisomy C through a familial translocation t(Cq+;Cq-)].
    Lejeune J, Rethoré MO, Berger R, Abonyi D, Dutrillaux B, See G.
    Ann Genet; 1968 Sep; 11(3):171-5. PubMed ID: 5304617
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  • 24. Developmental and other pathologic changes in syndromes caused by chromosome abnormalities.
    Gilbert EF, Opitz JM.
    Perspect Pediatr Pathol; 1982 Sep; 7():1-63. PubMed ID: 6214761
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  • 28. [Ring chromosome 14. II. A case report of r(14) mosaicism. The r(14) phenotype].
    Rethoré MO, Caille B, Huet de Barochez Y, de Blois MC, Ravel A, Lejeune J.
    Ann Genet; 1984 Sep; 27(2):91-5. PubMed ID: 6331796
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  • 29. [Ring chromosome 14. I. A case report on homogeneous r(14)].
    Raoul O, Razavi F, Lescs MC, Bouhanna A.
    Ann Genet; 1984 Sep; 27(2):88-90. PubMed ID: 6331795
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  • 30. [46,XY-45,X mosaicism and 18p- deletion].
    Giraud F, Hartung M, Mattei JF, Passeron P, Coignet J.
    Ann Genet; 1971 Mar; 14(1):59-62. PubMed ID: 5314297
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  • 32. Prenatal diagnosis and clinical features of an individual with tetrasomy 18p and trisomy 18q mosaicism.
    Habecker-Green JG, Naeem R, Gold H, O'Grady JP, Kanaan C, Bayer-Zwirello L, Murray MS, Cohn GM.
    J Perinatol; 1998 Mar; 18(5):395-8. PubMed ID: 9766419
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  • 35. A de novo tandem duplication 15(q21 leads to qter) mosaic.
    Yip MY, Parsons A, Hultén M.
    Clin Genet; 1982 Jul; 22(1):1-6. PubMed ID: 7172470
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  • 38. Phenotype/karyotype correlations of Y chromosome aneuploidy with emphasis on structural aberrations in postnatally diagnosed cases.
    Hsu LY.
    Am J Med Genet; 1994 Nov 01; 53(2):108-40. PubMed ID: 7856637
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