These tools will no longer be maintained as of December 31, 2024. Archived website can be found here. PubMed4Hh GitHub repository can be found here. Contact NLM Customer Service if you have questions.


Pubmed for Handhelds

PUBMED FOR HANDHELDS

Journal Abstract Search

472 related items for PubMed ID: 12215841

  • 1. Molecular analysis in true hermaphroditism: demonstration of low-level hidden mosaicism for Y-derived sequences in 46,XX cases.
    Queipo G, Zenteno JC, Peña R, Nieto K, Radillo A, Dorantes LM, Eraña L, Lieberman E, Söderlund D, Jiménez AL, Ramón G, Kofman-Alfaro S.
    Hum Genet; 2002 Sep; 111(3):278-83. PubMed ID: 12215841
    [Abstract] [Full Text] [Related]

  • 2. Molecular analysis in true hermaphrodites with different karyotypes and similar phenotypes.
    Torres L, López M, Méndez JP, Canto P, Cervantes A, Alfaro G, Pérez-Palacios G, Erickson RP, Kofman-Alfaro S.
    Am J Med Genet; 1996 May 17; 63(2):348-55. PubMed ID: 8725784
    [Abstract] [Full Text] [Related]

  • 3. [True hermaphroditism].
    Naito K.
    Nihon Rinsho; 2004 Feb 17; 62(2):300-4. PubMed ID: 14968535
    [Abstract] [Full Text] [Related]

  • 4. Molecular analysis of SRY gene in Brazilian 46,XX sex reversed patients: absence of SRY sequence in gonadal tissue.
    Domenice S, Nishi MY, Billerbeck AE, Carvalho FM, Frade EM, Latronico AC, Arnhold IJ, Mendonca BB.
    Med Sci Monit; 2001 Feb 17; 7(2):238-41. PubMed ID: 11257728
    [Abstract] [Full Text] [Related]

  • 5. Sex-determining genes on mouse autosomes identified by linkage analysis of C57BL/6J-YPOS sex reversal.
    Eicher EM, Washburn LL, Schork NJ, Lee BK, Shown EP, Xu X, Dredge RD, Pringle MJ, Page DC.
    Nat Genet; 1996 Oct 17; 14(2):206-9. PubMed ID: 8841197
    [Abstract] [Full Text] [Related]

  • 6. Familial case of 46,XX male and 46,XX true hermaphrodite associated with a paternal-derived SRY-bearing X chromosome.
    Abbas N, McElreavey K, Leconiat M, Vilain E, Jaubert F, Berger R, Nihoul-Fekete C, Rappaport R, Fellous M.
    C R Acad Sci III; 1993 Oct 17; 316(4):375-83. PubMed ID: 8402263
    [Abstract] [Full Text] [Related]

  • 7. 45,X/47,XXX/47,XX, del(Y)(p?)/46,XX mosaicism causing true hermaphroditism.
    Nieto K, Peña R, Palma I, Dorantes LM, Eraña L, Alvarez R, García-Cavazos R, Kofman-Alfaro S, Queipo G.
    Am J Med Genet A; 2004 Oct 15; 130A(3):311-4. PubMed ID: 15378545
    [Abstract] [Full Text] [Related]

  • 8. A point mutation, R59G, within the HMG-SRY box in a female 45,X/46,X, psu dic(Y)(pter-->q11::q11-->pter).
    Fernandez R, Marchal JA, Sanchez A, Pasaro E.
    Hum Genet; 2002 Sep 15; 111(3):242-6. PubMed ID: 12215836
    [Abstract] [Full Text] [Related]

  • 9. Partially deleted SRY gene confined to testicular tissue in a 46,XX true hermaphrodite without SRY in leukocytic DNA.
    Jiménez AL, Kofman-Alfaro S, Berumen J, Hernández E, Canto P, Méndez JP, Zenteno JC.
    Am J Med Genet; 2000 Aug 28; 93(5):417-20. PubMed ID: 10951467
    [Abstract] [Full Text] [Related]

  • 10. 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 28; 36(6):452-6. PubMed ID: 10874632
    [Abstract] [Full Text] [Related]

  • 11. [Molecular analysis of the Y chromosome in XX sex-reversed patients].
    Chernykh VB, Chukhrova AL, Vasserman NN, Il'ina EV, Karmanov ME, Fedotov VP, Poliakov AV.
    Genetika; 2008 Feb 28; 44(2):236-41. PubMed ID: 18619043
    [Abstract] [Full Text] [Related]

  • 12. [Cytogenetic analysis of four cases of hermaphroditism].
    Huang L, Xia J, Yang Y.
    Zhonghua Fu Chan Ke Za Zhi; 1995 May 28; 30(5):290-3. PubMed ID: 7648910
    [Abstract] [Full Text] [Related]

  • 13. A case of an intersex horse with 63,X/64,XX/65,XX,del(Y)(q?) karyotype.
    Bugno M, Zabek T, Golonka P, Pieńkowska-Schelling A, Schelling C, Słota E.
    Cytogenet Genome Res; 2008 May 28; 120(1-2):123-6. PubMed ID: 18467835
    [Abstract] [Full Text] [Related]

  • 14. Detection of Y-chromosome in gonadal tumours using fluorescence in situ hybridization: diagnostic value in intersex conditions including older patients with clinically unsuspected androgen insensitivity syndrome.
    Stewart CJ, Baker E, Beaton C, Crook M, Peverall J, Wallace S.
    Histopathology; 2008 Jan 28; 52(2):175-82. PubMed ID: 18184266
    [Abstract] [Full Text] [Related]

  • 15. Up-regulation of SOX9 in human sex-determining region on the Y chromosome (SRY)-negative XX males.
    Kojima Y, Hayashi Y, Mizuno K, Sasaki S, Fukui Y, Koopman P, Morohashi K, Kohri K.
    Clin Endocrinol (Oxf); 2008 May 28; 68(5):791-9. PubMed ID: 17986281
    [Abstract] [Full Text] [Related]

  • 16. Clinical and molecular cytogenetic studies in three infertile patients with mosaic rearranged Y chromosomes.
    Bettio D, Venci A, Rizzi N, Negri L, Setti PL.
    Hum Reprod; 2006 Apr 28; 21(4):972-5. PubMed ID: 16484313
    [Abstract] [Full Text] [Related]

  • 17. 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]

  • 18.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 19. 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]

  • 20.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

    Page: [Next] [New Search]
    of 24.