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

267 related items for PubMed ID: 16708803

  • 1. [Confirmation of the extra small chromosome in abnormality karyotype by PCR and FISH].
    Xue ZG, Li YM, Yao ZY, Long ZG, Dai HP, Wu LQ, Xia K, Xia JH.
    Zhong Nan Da Xue Xue Bao Yi Xue Ban; 2005 Dec; 30(6):657-9. PubMed ID: 16708803
    [Abstract] [Full Text] [Related]

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

  • 3. [An investigation of small marker chromosome in eight Turner syndrome patients by fluorescence in situ hybridization and DNA analysis].
    Hu X, Zhu B, Hu B, Lin H, Shu D, Li C, Liu X.
    Zhonghua Yi Xue Yi Chuan Xue Za Zhi; 1999 Dec; 16(6):392-4. PubMed ID: 10581353
    [Abstract] [Full Text] [Related]

  • 4. [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]

  • 5.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 6.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 7.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

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

  • 9.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 10. [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 Aug; 47(2):117-25. PubMed ID: 7610280
    [Abstract] [Full Text] [Related]

  • 11. 47,XXY female with testicular feminization and positive SRY: a case report.
    Saavedra-Castillo E, Cortés-Gutiérrez EI, Dávila-Rodríguez MI, Reyes-Martínez ME, Oliveros-Rodríguez A.
    J Reprod Med; 2005 Feb; 50(2):138-40. PubMed ID: 15755052
    [Abstract] [Full Text] [Related]

  • 12. 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; 62(Pt 2):99-106. PubMed ID: 9759471
    [Abstract] [Full Text] [Related]

  • 13. 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]

  • 14. 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]

  • 15.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 16. [Application of fluorescence in situ hybridization in the diagnosis of genetic diseases].
    Zhao L, Li H, Xue YQ, Pan JL, Wu YF, Lu M.
    Zhonghua Yi Xue Yi Chuan Xue Za Zhi; 2004 Dec 27; 21(6):611-4. PubMed ID: 15583994
    [Abstract] [Full Text] [Related]

  • 17. Novel karyotype in the Ullrich-Turner syndrome--45,X/46,X,r(X)/46,X, dic(X)--investigated with fluorescence in situ hybridization.
    Robson L, Jackson J, Cowell C, Sillence D, Smith A.
    Am J Med Genet; 1994 Apr 15; 50(3):251-4. PubMed ID: 8042669
    [Abstract] [Full Text] [Related]

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

  • 19. Molecular detection of cryptic Y-chromosomal material in patients with Turner syndrome.
    Cortés-Gutiérrez EI, Herrera-Bartolo R, Dávila-Rodríguez MI, Palacios-Saucedo GC, Vargas-Villarreal J, Romero-Villarreal JB.
    Oncol Rep; 2012 Oct 15; 28(4):1205-10. PubMed ID: 22824904
    [Abstract] [Full Text] [Related]

  • 20. Different chromosome Y abnormalities in Turner syndrome.
    Bağci G, Acar H, Tomruk H.
    Genet Couns; 2001 Oct 15; 12(3):255-61. PubMed ID: 11693789
    [Abstract] [Full Text] [Related]

    Page: [Next] [New Search]
    of 14.