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Journal Abstract Search

165 related items for PubMed ID: 3066281

  • 1. Trisomy 8p by malsegregation of a t(5;8)(p15;p11)mat in a case of XY pure gonadal dysgenesis.
    Memo L, Lenzini E, Baccichetti C.
    Ann Genet; 1988; 31(3):181-5. PubMed ID: 3066281
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  • 2. [Swyer syndrome. Apropos of a new case of pure gonadal dysgenesis with Karyotype 46 XY].
    Cossard F, Saurel J, Berger-Pauquet M, Brun G.
    J Gynecol Obstet Biol Reprod (Paris); 1984; 13(2):151-6. PubMed ID: 6736590
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  • 3. [Quality of life in the patients with disorders of sexual development and with Y chromosome in karyotype].
    Lisá L.
    Cas Lek Cesk; 2007; 146(3):215-7. PubMed ID: 17419302
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  • 4. [Translocation (3;20) and anorchism].
    Gilgenkrantz S, Cruz-Marin F, Gregoire MJ, Walter S, Pierson M.
    J Genet Hum; 1981 Sep; 29(3):321-7. PubMed ID: 7334352
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  • 5. 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 Sep; 33(4):342-7. PubMed ID: 7186725
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  • 11. Management of phenotypic female patients with an XY karyotype.
    Portuondo JA, Neyro JL, Barral A, Gonzalez-Gorospe F, Benito JA.
    J Reprod Med; 1986 Jul; 31(7):611-5. PubMed ID: 3091820
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  • 13. XY gonadal dysgenesis: aberrant testicular differentiation in the presence of H-Y antigen.
    Moltz L, Schwartz U, Pickartz H, Hammerstein J, Wolf U.
    Obstet Gynecol; 1981 Jul; 58(1):17-25. PubMed ID: 7195530
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  • 14. Genetic heterogeneity of XY gonadal dysgenesis (Swyer syndrome): H-Y antigen-negative XY gonadal dysgenesis associated with inflammatory bowel disease.
    Passarge E, Wolf U.
    Am J Med Genet; 1981 Jul; 8(4):437-41. PubMed ID: 7246614
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  • 15. [Mesomelic dwarfism Langer type associated to mixed gonadal dysgenesis, whit cariotipe 46,XY/45 X (author's transl)].
    Ruíz Gómez MJ, Martínez González M, Machín Jiménez AR, Fernández Villahoz AL.
    An Esp Pediatr; 1979 Dec; 12(12):897-904. PubMed ID: 533057
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  • 17. Pure partial trisomy 5q33-->5q35 resulting from the adjacent-1 segregation of a paternal (5;14)(q33;p12) translocation.
    Paoloni-Giacobino A, Bottani A, Dahoun SP.
    Ann Genet; 1999 Dec; 42(3):166-9. PubMed ID: 10526660
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