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PUBMED FOR HANDHELDS

Journal Abstract Search


138 related items for PubMed ID: 11424145

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  • 2. Familial occurrence of agonadism and multiple internal malformations in phenotypically normal girls with 46,XY and 46,XX karyotypes, respectively: a new autosomal recessive syndrome.
    Kennerknecht I, Sorgo W, Oberhoffer R, Teller WM, Mattfeldt T, Negri G, Vogel W.
    Am J Med Genet; 1993 Dec 01; 47(8):1166-70. PubMed ID: 8291549
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  • 4. Female external genitalia, absent uterus, and probable agonadism in a 46,XY infant with bilateral upper amelia.
    Ohro Y, Suzuki Y, Tsutsumi Y, Ogata T.
    Clin Genet; 1998 Jul 01; 54(1):52-5. PubMed ID: 9727740
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  • 5. Agonadism in a 46,XY patient with CHARGE association.
    Kushnick T, Wiley JE, Palmer SM.
    Am J Med Genet; 1992 Jan 01; 42(1):96-9. PubMed ID: 1308372
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  • 6. Female external genitalia and müllerian duct derivatives in a 46,XY infant with the smith-lemli-Opitz syndrome.
    Bialer MG, Penchaszadeh VB, Kahn E, Libes R, Krigsman G, Lesser ML.
    Am J Med Genet; 1987 Nov 01; 28(3):723-31. PubMed ID: 3322011
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  • 7. Gonadal agenesis in XX and XY sisters: evidence for the involvement of an autosomal gene.
    Mendonça BB, Barbosa AS, Arnhold IJ, McElreavey K, Fellous M, Moreira-Filho CA.
    Am J Med Genet; 1994 Aug 01; 52(1):39-43. PubMed ID: 7977459
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  • 9. Agonadism in two sisters with XY gonosomal constitution, mental retardation, short stature, severely retarded bone age, and multiple extragenital malformations: a new autosomal recessive syndrome.
    Kennerknecht I, von Saurma P, Brenner R, Just W, Barbi G, Sorgo W, Heinze E, Wolf AS, Schneider V, Günther KP.
    Am J Med Genet; 1995 Oct 23; 59(1):62-7. PubMed ID: 8849014
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  • 10. Embryonic testicular regression syndrome: variable phenotypic expression in siblings.
    Josso N, Briard ML.
    J Pediatr; 1980 Aug 23; 97(2):200-4. PubMed ID: 7400886
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  • 14. [Causes of ambiguous external genitalia in neonates].
    Zdravković D, Milenković T, Sedlecki K, Guć-Sćekić M, Rajić V, Banićević M.
    Srp Arh Celok Lek; 2001 Aug 23; 129(3-4):57-60. PubMed ID: 11534268
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  • 16. Seckel-like syndrome in three siblings.
    Arnold SR, Spicer D, Kouseff B, Lacson A, Gilbert-Barness E.
    Pediatr Dev Pathol; 1999 Aug 23; 2(2):180-7. PubMed ID: 9949225
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  • 17. Report of a kindred with X-linked (or autosomal dominant sex-limited) 46,XY partial gonadal dysgenesis.
    Fechner PY, Marcantonio SM, Ogata T, Rosales TO, Smith KD, Goodfellow PN, Migeon CJ, Berkovitz GD.
    J Clin Endocrinol Metab; 1993 May 23; 76(5):1248-53. PubMed ID: 8496317
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  • 18. Embryonic testicular regression syndrome and severe mental retardation in sibs.
    de Grouchy J, Gompel A, Salomon-Bernard Y, Kuttenn F, Yaneva H, Paniel JB, Le Merrer M, Roubin M, Doussau de Bazignan M, Turleau C.
    Ann Genet; 1985 May 23; 28(3):154-60. PubMed ID: 3879148
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