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Journal Abstract Search

347 related items for PubMed ID: 1218222

  • 1. Sex chromosome mosaicism of X/XY or X/XY/XYY.
    Wilson MG, Ebbin AJ, Shinno NW, Towner JW.
    Birth Defects Orig Artic Ser; 1975; 11(5):255-66. PubMed ID: 1218222
    [Abstract] [Full Text] [Related]

  • 2. [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; 129(3-4):57-60. PubMed ID: 11534268
    [Abstract] [Full Text] [Related]

  • 3. A Turner-like phenotype in a girl with an isodicentric fluorescent Y chromosome mosaicism.
    Bergendi E, Plöchl E, Vlasak I, Rittinger O, Muss W.
    Klin Padiatr; 1997; 209(3):133-6. PubMed ID: 9183775
    [Abstract] [Full Text] [Related]

  • 4. Gonadoblastoma in Turner syndrome patients with nonmosaic 45,X karyotype and Y chromosome sequences.
    Canto P, Kofman-Alfaro S, Jiménez AL, Söderlund D, Barrón C, Reyes E, Méndez JP, Zenteno JC.
    Cancer Genet Cytogenet; 2004 Apr 01; 150(1):70-2. PubMed ID: 15041227
    [Abstract] [Full Text] [Related]

  • 5. Laparoscopy in endocrine and genetic disorders of the gonads.
    Minozzi M, Faggiano M, Jori GP, Lombardi G.
    Acta Endocrinol Suppl (Copenh); 1975 Apr 01; 192():1-124. PubMed ID: 123111
    [Abstract] [Full Text] [Related]

  • 6. Phenotype/karyotype correlations of Y chromosome aneuploidy with emphasis on structural aberrations in postnatally diagnosed cases.
    Hsu LY.
    Am J Med Genet; 1994 Nov 01; 53(2):108-40. PubMed ID: 7856637
    [Abstract] [Full Text] [Related]

  • 7. 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 Nov 01; 20(2):173-9. PubMed ID: 19650415
    [Abstract] [Full Text] [Related]

  • 8. Gonadoblastoma and Turner syndrome.
    Brant WO, Rajimwale A, Lovell MA, Travers SH, Furness PD, Sorensen M, Oottamasathien S, Koyle MA.
    J Urol; 2006 May 01; 175(5):1858-60. PubMed ID: 16600779
    [Abstract] [Full Text] [Related]

  • 9. SRY gene increases the risk of developing gonadoblastoma and/or nontumoral gonadal lesions in Turner syndrome.
    Bianco B, Lipay M, Guedes A, Oliveira K, Verreschi IT.
    Int J Gynecol Pathol; 2009 Mar 01; 28(2):197-202. PubMed ID: 19188812
    [Abstract] [Full Text] [Related]

  • 10. [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 Mar 01; 15(2):89-100. PubMed ID: 15524154
    [Abstract] [Full Text] [Related]

  • 11. Distribution of sex chromosomes in dysgenetic gonads of mixed type.
    Röpke A, Kalinski T, Mohnike K, Sel S, Jakubiczka S, Pelz AF, Roessner A, Wieacker PF.
    Cytogenet Genome Res; 2007 Mar 01; 116(1-2):146-51. PubMed ID: 17268195
    [Abstract] [Full Text] [Related]

  • 12. Mixed gonadal dysgenesis.
    Zäh W, Kalderon AE, Tucci JR.
    Acta Endocrinol Suppl (Copenh); 1975 Mar 01; 197():1-39. PubMed ID: 1094776
    [Abstract] [Full Text] [Related]

  • 13. Sex chromosomal mosaicism in the gonads of patients with gonadal dysgenesis, but normal female or male karyotypes in lymphocytes.
    Röpke A, Pelz AF, Volleth M, Schlösser HW, Morlot S, Wieacker PF.
    Am J Obstet Gynecol; 2004 Apr 01; 190(4):1059-62. PubMed ID: 15118641
    [Abstract] [Full Text] [Related]

  • 14. PCR detection of Y-specific sequences in patients with Ullrich-Turner syndrome: clinical implications and limitations.
    Osipova GR, Karmanov ME, Kozlova SI, Evgrafov OV.
    Am J Med Genet; 1998 Apr 01; 76(4):283-7. PubMed ID: 9545090
    [Abstract] [Full Text] [Related]

  • 15. 45,X/46,XY/47,XYY mosaicism in a phenotypic female with gonadoblastoma.
    Osztovics M, Ivády G, Ruzicska P, Bühler EM, Király L.
    Acta Paediatr Acad Sci Hung; 1974 Apr 01; 15(3-4):295-9. PubMed ID: 4469141
    [Abstract] [Full Text] [Related]

  • 16. Analysis of the SRY gene in a girl with 45,X/46,XY genotype.
    Akbas E, Soylemez F, Hallioglu O, Polat S, Turkoz G.
    Genet Couns; 2009 Apr 01; 20(3):249-54. PubMed ID: 19852431
    [Abstract] [Full Text] [Related]

  • 17. Detection of Y chromosome sequences in a 45,X/46,XXq--patient by Southern blot analysis of PCR-amplified DNA and fluorescent in situ hybridization (FISH).
    Kocova M, Siegel SF, Wenger SL, Lee PA, Nalesnik M, Trucco M.
    Am J Med Genet; 1995 Feb 13; 55(4):483-8. PubMed ID: 7762591
    [Abstract] [Full Text] [Related]

  • 18. Autosomal/heterosomal mixoploids: a report on two patients, a female with a 45, Z/47,XX plus 21 and a male with A 45,X/47,XY, plus 21 chromosome constitution.
    Hustinx TW, Haar BG, Scheres JM, Rutten FJ.
    Ann Genet; 1974 Dec 13; 17(4):225-34. PubMed ID: 4281287
    [No Abstract] [Full Text] [Related]

  • 19. The spectrum of 45,X/46,XY mosaicism in Taiwanese children: The experience of a single center.
    Huang YC, Lee CT, Wu MZ, Liu SY, Tung YC, Ho HN, Tsai WY.
    J Formos Med Assoc; 2019 Jan 13; 118(1 Pt 3):450-456. PubMed ID: 30017534
    [Abstract] [Full Text] [Related]

  • 20. G-11 staining in Turner's syndrome with mos 45,X/46,X,r(?).
    de Almeida JC, Llerena JC, Molina Gomes D, Rita Martins R, Jung M, Reis DF, Cunha AG.
    Ann Genet; 1985 Jan 13; 28(1):37-41. PubMed ID: 2409888
    [Abstract] [Full Text] [Related]

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