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162 related items for PubMed ID: 10738532

  • 1. Mosaic Turner syndrome: cytogenetics versus FISH.
    Abulhasan SJ, Tayel SM, al-Awadi SA.
    Ann Hum Genet; 1999 May; 63(Pt 3):199-206. PubMed ID: 10738532
    [Abstract] [Full Text] [Related]

  • 2. Different chromosome Y abnormalities in Turner syndrome.
    Bağci G, Acar H, Tomruk H.
    Genet Couns; 2001 May; 12(3):255-61. PubMed ID: 11693789
    [Abstract] [Full Text] [Related]

  • 3. Evaluation of sex chromosome aneuploidies in women with Turner's syndrome by G-banding and FISH. A serial case study.
    Cortés-Gutiérrez EI, Cerda-Flores RM, Silva-Cudish JB, Dávila-Rodríguez MI, Hernández-Herrera R, Leal-Garza CH.
    J Reprod Med; 2003 Oct; 48(10):804-8. PubMed ID: 14628733
    [Abstract] [Full Text] [Related]

  • 4. [Identification of sex chromosome markers using fluorescence in situ hybridization (FISH)].
    González-del-Angel A, Blanco B, del Castillo V, Carnevale A.
    Rev Invest Clin; 1995 Oct; 47(2):117-25. PubMed ID: 7610280
    [Abstract] [Full Text] [Related]

  • 5. [Marker chromosome analysis in Chinese patients with Turner syndrome by fluorescence in situ hybridization].
    Liang Y, Luo XP.
    Zhonghua Yi Xue Yi Chuan Xue Za Zhi; 2005 Aug; 22(4):435-7. PubMed ID: 16086285
    [Abstract] [Full Text] [Related]

  • 6. Molecular cytogenetic characterization of two Turner syndrome patients with mosaic ring X chromosome.
    Chauhan P, Jaiswal SK, Lakhotia AR, Rai AK.
    J Assist Reprod Genet; 2016 Sep; 33(9):1161-8. PubMed ID: 27387888
    [Abstract] [Full Text] [Related]

  • 7. X microchromosome with additional chromosome anomalies found in Ullrich-Turner syndrome.
    Wydner KL, Li M, Singer-Granick C, Sciorra LJ, Krueger LJ.
    Am J Med Genet; 1995 Mar 27; 56(2):141-6. PubMed ID: 7625435
    [Abstract] [Full Text] [Related]

  • 8. Prenatal diagnosis of 45,X and 45,X mosaicism: the need for thorough cytogenetic and clinical evaluations.
    Huang B, Thangavelu M, Bhatt S, J Sandlin C, Wang S.
    Prenat Diagn; 2002 Feb 27; 22(2):105-10. PubMed ID: 11857613
    [Abstract] [Full Text] [Related]

  • 9. Analysis of sex chromosome aneuploidy in 41 patients with Turner syndrome: a study of 'hidden' mosaicism.
    Fernández-García R, García-Doval S, Costoya S, Pásaro E.
    Clin Genet; 2000 Sep 27; 58(3):201-8. PubMed ID: 11076042
    [Abstract] [Full Text] [Related]

  • 10. High frequency of tissue-specific mosaicism in Turner syndrome patients.
    Nazarenko SA, Timoshevsky VA, Sukhanova NN.
    Clin Genet; 1999 Jul 27; 56(1):59-65. PubMed ID: 10466418
    [Abstract] [Full Text] [Related]

  • 11. A non-sex chromosome marker in a patient with an atypical Ullrich-Turner phenotype and mosaicism of 46,X,mar/46,XX.
    Gray BA, Bent-Williams A, Wolff DJ, Zori RT.
    Clin Genet; 2001 Jul 27; 60(1):73-6. PubMed ID: 11531974
    [Abstract] [Full Text] [Related]

  • 12. Turner syndrome: a study of chromosomal mosaicism.
    Fernández R, Méndez J, Pásaro E.
    Hum Genet; 1996 Jul 27; 98(1):29-35. PubMed ID: 8682502
    [Abstract] [Full Text] [Related]

  • 13. Cytogenetic and molecular investigations of Y chromosome sequences and their role in Turner syndrome.
    Quilter CR, Taylor K, Conway GS, Nathwani N, Delhanty JD.
    Ann Hum Genet; 1998 Mar 27; 62(Pt 2):99-106. PubMed ID: 9759471
    [Abstract] [Full Text] [Related]

  • 14. FISH analysis helps identify low-level mosaicism in Ullrich-Turner syndrome patients.
    Wiktor A, Van Dyke DL.
    Genet Med; 2004 Mar 27; 6(3):132-5. PubMed ID: 15354330
    [Abstract] [Full Text] [Related]

  • 15. [Diagnosis of sex chromosome abnormality by fluorescence in-situ hybridization].
    Huang Y, Sun X, Li Q.
    Zhonghua Yi Xue Za Zhi; 1999 Feb 27; 79(2):106-8. PubMed ID: 11601014
    [Abstract] [Full Text] [Related]

  • 16. [Down-Turner syndrome (45,X/47,XY,+21): case report and review].
    Ryu SW, Lee G, Baik CS, Shim SH, Kim JT, Lee JS, Lee KA.
    Korean J Lab Med; 2010 Apr 27; 30(2):195-200. PubMed ID: 20445340
    [Abstract] [Full Text] [Related]

  • 17. A variant Klinefelter syndrome patient with an XXY/XX/XY karyotype studied by GTG-banding and fluorescence in situ hybridization.
    Mark HF, Bai H, Sotomayor E, Mark S, Zolnierz K, Airall E, Sigman M.
    Exp Mol Pathol; 1999 Sep 27; 67(1):50-6. PubMed ID: 10493892
    [Abstract] [Full Text] [Related]

  • 18. Cytogenetic and molecular findings in patients with Turner's syndrome stigmata.
    Kuznetzova T, Baranov A, Schwed N, Ivaschenko T, Malet P, Giollant M, Savitsky GA, Baranov V.
    J Med Genet; 1995 Dec 27; 32(12):962-7. PubMed ID: 8825925
    [Abstract] [Full Text] [Related]

  • 19. [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 Dec 27; 15(2):89-100. PubMed ID: 15524154
    [Abstract] [Full Text] [Related]

  • 20. [Use of molecular cytogenetic techniques for establishing the origin of chromosome markers in patients with Turner phenotype].
    Bocian E, Stańczak H, Wiśniewski A, Mazurczak T, Stankiewicz P.
    Pediatr Pol; 1996 Mar 27; 71(3):203-9. PubMed ID: 8966091
    [Abstract] [Full Text] [Related]

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