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Journal Abstract Search

322 related items for PubMed ID: 9249610

  • 1. Detection of SRY in a 46,XY female (Swyer's syndrome).
    Imai A, Horibe S, Fuseya T, Takagi H, Tamaya T.
    J Med; 1997; 28(1-2):49-54. PubMed ID: 9249610
    [Abstract] [Full Text] [Related]

  • 2. Complete XY gonadal dysgenesis and aspects of the SRYgenotype and gonadal tumor formation.
    Uehara S, Hashiyada M, Sato K, Nata M, Funato T, Okamura K.
    J Hum Genet; 2002; 47(6):279-84. PubMed ID: 12111377
    [Abstract] [Full Text] [Related]

  • 3. Mutational analysis of SRY in XY females.
    Hawkins JR.
    Hum Mutat; 1993; 2(5):347-50. PubMed ID: 8257986
    [Abstract] [Full Text] [Related]

  • 4. Genetic evidence equating SRY and the testis-determining factor.
    Berta P, Hawkins JR, Sinclair AH, Taylor A, Griffiths BL, Goodfellow PN, Fellous M.
    Nature; 1990 Nov 29; 348(6300):448-50. PubMed ID: 2247149
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  • 5. [Molecular studies of chromosome Y in 20 patients with 46,XY karyotype].
    Ben Jemaa Khemakhem L, Hila L, Mrad R, Maazoul F, Chaabouni H.
    Tunis Med; 1997 Oct 29; 75(10):762-7. PubMed ID: 9507345
    [No Abstract] [Full Text] [Related]

  • 6. Description and functional implications of a novel mutation in the sex-determining gene SRY.
    Poulat F, Soullier S, Gozé C, Heitz F, Calas B, Berta P.
    Hum Mutat; 1994 Oct 29; 3(3):200-4. PubMed ID: 8019555
    [Abstract] [Full Text] [Related]

  • 7. Independent observation of SRY mutation I90M in a patient with complete gonadal dysgenesis.
    Dörk T, Stuhrmann M, Miller K, Schmidtke J.
    Hum Mutat; 1998 Oct 29; 11(1):90-1. PubMed ID: 9450909
    [No Abstract] [Full Text] [Related]

  • 8. The role of sexual related Y gene detection in the diagnosis of patients with gonadal dysgenesis.
    Yu Q, Huang S, Ye L, Feng L, He F, Ye J, Gu C, Ge Q.
    Chin Med J (Engl); 2001 Feb 29; 114(2):128-31. PubMed ID: 11780190
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  • 10. Human chromosome Y and SRY.
    Shah VC, Smart V.
    Cell Biol Int; 1996 Jan 29; 20(1):3-6. PubMed ID: 8936401
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  • 15. Analysis of the testis-determining gene SRY in patients with XY gonadal dysgenesis.
    Tsutsumi O, Iida T, Nakahori Y, Taketani Y.
    Horm Res; 1996 Jan 29; 46 Suppl 1():6-10. PubMed ID: 8864741
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  • 17. Mutation analysis of the 2 kb 5' to SRY in XY females and XY intersex subjects.
    Kwok C, Tyler-Smith C, Mendonca BB, Hughes I, Berkovitz GD, Goodfellow PN, Hawkins JR.
    J Med Genet; 1996 Jun 29; 33(6):465-8. PubMed ID: 8782045
    [Abstract] [Full Text] [Related]

  • 18. Structural basis for SRY-dependent 46-X,Y sex reversal: modulation of DNA bending by a naturally occurring point mutation.
    Murphy EC, Zhurkin VB, Louis JM, Cornilescu G, Clore GM.
    J Mol Biol; 2001 Sep 21; 312(3):481-99. PubMed ID: 11563911
    [Abstract] [Full Text] [Related]

  • 19. Combined Leydig cell and Sertoli cell dysfunction in 46,XX males lacking the sex determining region Y gene.
    Turner B, Fechner PY, Fuqua JS, Marcantonio SM, Perlman EJ, Vordermark JS, Berkovitz GD.
    Am J Med Genet; 1995 Jul 03; 57(3):440-3. PubMed ID: 7677147
    [Abstract] [Full Text] [Related]

  • 20. Epigenetic abnormality of SRY gene in the adult XY female with pericentric inversion of the Y chromosome.
    Mitsuhashi T, Warita K, Sugawara T, Tabuchi Y, Takasaki I, Kondo T, Hayashi F, Wang ZY, Matsumoto Y, Miki T, Takeuchi Y, Ebina Y, Yamada H, Sakuragi N, Yokoyama T, Nanmori T, Kitagawa H, Kant JA, Hoshi N.
    Congenit Anom (Kyoto); 2010 Jun 03; 50(2):85-94. PubMed ID: 20184645
    [Abstract] [Full Text] [Related]

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