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Journal Abstract Search


108 related items for PubMed ID: 9128931

  • 1. Cytogenetic and molecular studies of a familial paracentric inversion of Y chromosome present in a patient with ambiguous genitalia.
    Liou JD, Ma YY, Gibson LH, Su H, Charest N, Lau YF, Yang-Feng TL.
    Am J Med Genet; 1997 May 16; 70(2):134-7. PubMed ID: 9128931
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  • 2. Partial gonadal dysgenesis in a patient with a marker Y chromosome.
    Fechner PY, Smith KD, Jabs EW, Migeon CJ, Berkovitz GD.
    Am J Med Genet; 1992 Apr 01; 42(6):807-12. PubMed ID: 1313209
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  • 3. XY sex reversal and gonadal dysgenesis due to 9p24 monosomy.
    McDonald MT, Flejter W, Sheldon S, Putzi MJ, Gorski JL.
    Am J Med Genet; 1997 Dec 19; 73(3):321-6. PubMed ID: 9415692
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  • 4. 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 19; 50(2):85-94. PubMed ID: 20184645
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  • 5. Heterogeneity of pericentric inversions of the human y chromosome.
    Knebel S, Pasantes JJ, Thi DA, Schaller F, Schempp W.
    Cytogenet Genome Res; 2011 Jun 19; 132(4):219-26. PubMed ID: 21307635
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  • 6. Use of a probe for the putative sex determining gene, zinc finger Y, in the study of patients with ambiguous genitalia and XY gonadal dysgenesis.
    Erickson RP, Verga V, Dasouki M.
    Am J Med Genet; 1990 Jun 19; 36(2):232-6. PubMed ID: 2368811
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  • 7. Coexistence of inverted Y, chromosome 15p+ and abnormal phenotype.
    Acar H, Cora T, Erkul I.
    Genet Couns; 1999 Jun 19; 10(2):163-70. PubMed ID: 10422010
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  • 9. XX sex reversal: molecular analysis of the SRY/ZFY regions.
    Reddy PP, Papenhausen PR, Suh YM, Riddick LM, Calvano CJ, Mandell J.
    J Urol; 1997 Sep 19; 158(3 Pt 2):1305-7. PubMed ID: 9258201
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  • 10. Isodicentric Y (p11.32) chromosome in an infant with mixed gonadal dysgenesis.
    Aktas D, Alikasifoglu M, Gonc N, Senocak ME, Tuncbilek E.
    Eur J Med Genet; 2006 Sep 19; 49(2):141-9. PubMed ID: 16530711
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  • 12. [Screening for Y chromosome sequences in patients with Turner syndrome].
    Ferrão L, Lopes ML, Limbert C, Marques B, Boieiro F, Silva M, Marques R, Lavinha J, Mota A, Gonçalves J.
    Acta Med Port; 2002 Sep 19; 15(2):89-100. PubMed ID: 15524154
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  • 13. 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 Sep 19; 47(6):279-84. PubMed ID: 12111377
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  • 14. FISH mapping of the sex-reversal region on human chromosome 9p in two XY females and in primates.
    Shan Z, Zabel B, Trautmann U, Hillig U, Ottolenghi C, Wan Y, Haaf T.
    Eur J Hum Genet; 2000 Mar 19; 8(3):167-73. PubMed ID: 10780781
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  • 16. [Molecular sex determination. Significance in the diagnosis of gonadal pathologies].
    Copelli S, Targovnik H, Bergada C.
    Medicina (B Aires); 1995 Mar 19; 55(6):705-11. PubMed ID: 8731584
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  • 17. An XX male with the sex-determining region Y gene inserted in the long arm of chromosome 16.
    Dauwerse JG, Hansson KB, Brouwers AA, Peters DJ, Breuning MH.
    Fertil Steril; 2006 Aug 19; 86(2):463.e1-5. PubMed ID: 16769064
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  • 18. Mixed gonadal dysgenesis with 45,X/46,X,idic(Y)/46,XY,idic(Y) karyotype.
    Caglayan AO, Demiryilmaz F, Kendirci M, Ozyazgan I, Akalin H, Bittmann S.
    Genet Couns; 2009 Aug 19; 20(2):173-9. PubMed ID: 19650415
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  • 20. Incomplete masculinisation of XX subjects carrying the SRY gene on an inactive X chromosome.
    Kusz K, Kotecki M, Wojda A, Szarras-Czapnik M, Latos-Bielenska A, Warenik-Szymankiewicz A, Ruszczynska-Wolska A, Jaruzelska J.
    J Med Genet; 1999 Jun 19; 36(6):452-6. PubMed ID: 10874632
    [Abstract] [Full Text] [Related]


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