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Journal Abstract Search

204 related items for PubMed ID: 7805169

  • 1. [Molecular cytogenetic study of Turner's syndrome with the 45, X/46,X,r(?) karyotype].
    Shi Y, Shi H, Ma S.
    Zhongguo Yi Xue Ke Xue Yuan Xue Bao; 1994 Jun; 16(3):218-21. PubMed ID: 7805169
    [Abstract] [Full Text] [Related]

  • 2. Identification of the origin of ring/marker chromosomes in patients with Ullrich-Turner syndrome using X and Y specific alpha satellite DNA probes.
    Tharapel SA, Wilroy RS, Keath AM, Rivas ML, Tharapel AT.
    Am J Med Genet; 1992 Mar 01; 42(5):720-3. PubMed ID: 1632446
    [Abstract] [Full Text] [Related]

  • 3. [Analysis of the small supernumerary marker chromosome in Turner syndrome with 45, X/46, X, + mar karyotype].
    Ye ZC, Cai JG, Zhu XY, Zhao R, He XY, Zhong Y, Liu KX, Zhu YM.
    Zhonghua Yi Xue Yi Chuan Xue Za Zhi; 2009 Aug 01; 26(4):461-4. PubMed ID: 20017317
    [Abstract] [Full Text] [Related]

  • 4. [Identification and characterization of marker chromosome in Turner syndrome].
    Tan YQ, Cheng DH, DI YF, Li LY, Lu GX.
    Zhonghua Fu Chan Ke Za Zhi; 2007 Oct 01; 42(10):679-82. PubMed ID: 18241543
    [Abstract] [Full Text] [Related]

  • 5. 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 01; 48(10):804-8. PubMed ID: 14628733
    [Abstract] [Full Text] [Related]

  • 6. A boy with small supernumerary marker chromosome X identified by FISH.
    Koç A, Yirmibeş Karaoğuz M, Pala E, Kan D, Karaer K, Gücüyener K, Perçin EF.
    Genet Couns; 2007 Oct 01; 18(4):393-9. PubMed ID: 18286820
    [Abstract] [Full Text] [Related]

  • 7. [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 01; 71(3):203-9. PubMed ID: 8966091
    [Abstract] [Full Text] [Related]

  • 8. A case of 46,XX,r(X) (p1q1) diagnosed by in situ hybridization.
    Koch J, Kølvraa S, Hobolt N, Petersen GB, Willard HF, Waye JS, Gregersen N, Bolund L.
    Clin Genet; 1990 Mar 01; 37(3):216-20. PubMed ID: 2323091
    [Abstract] [Full Text] [Related]

  • 9. [Identification of the small supernumerary marker chromosomes in two patients with Turner syndrome].
    Wen J, Liang D, Liao X, Xue J, Tang G, Xia Y, Long Z, Dai H, Wu L.
    Zhonghua Yi Xue Yi Chuan Xue Za Zhi; 2009 Dec 01; 26(6):659-63. PubMed ID: 19953489
    [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 Dec 01; 47(2):117-25. PubMed ID: 7610280
    [Abstract] [Full Text] [Related]

  • 11. 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 Dec 01; 28(1):37-41. PubMed ID: 2409888
    [Abstract] [Full Text] [Related]

  • 12. Cytogenetic findings in Serbian patients with Turner's syndrome stigmata.
    Djordjević VA, Jovanović JV, Pavković-Lučić SB, Drakulić DD, Djurović MM, Gotić MD.
    Genet Mol Res; 2010 Nov 09; 9(4):2213-21. PubMed ID: 21064029
    [Abstract] [Full Text] [Related]

  • 13. 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]

  • 14. [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 15; 22(4):435-7. PubMed ID: 16086285
    [Abstract] [Full Text] [Related]

  • 15. [A report of 2 cases of Turner's syndrome with a ring X chromosome].
    Migliori MV, Bartolotta E, Maurizi M, Bonazzi P, Cardinale G, Manunza V.
    Minerva Pediatr; 1991 Sep 15; 43(9):605-9. PubMed ID: 1758399
    [Abstract] [Full Text] [Related]

  • 16. An atypical Turner syndrome patient with ring X chromosome mosaicism.
    Cantú ES, Jacobs DF, Pai GS.
    Ann Clin Lab Sci; 1995 Sep 15; 25(1):60-5. PubMed ID: 7762970
    [Abstract] [Full Text] [Related]

  • 17. Determining the origins and the structural aberrations of small marker chromosomes in two cases of 45,X/46,X, + mar by use of chromosome-specific DNA probes.
    Lin CC, Meyne J, Sasi R, Bowen P, Unger T, Tainaka T, Hadro TA, Hoo JJ.
    Am J Med Genet; 1990 Sep 15; 37(1):71-8. PubMed ID: 2240047
    [Abstract] [Full Text] [Related]

  • 18. [Detection of mosaicism in women with Turner's syndrome using fluorescence in situ hybridization].
    Zemanová Z, Musilová J, Kurková S, Mayerová K, Pacovská K, Michalová K.
    Cas Lek Cesk; 1999 Jun 28; 138(13):396-400. PubMed ID: 10566209
    [Abstract] [Full Text] [Related]

  • 19. An investigation of ring and dicentric chromosomes found in three Turner's syndrome patients using DNA analysis and in situ hybridisation with X and Y chromosome specific probes.
    Cooper C, Crolla JA, Laister C, Johnston DI, Cooke P.
    J Med Genet; 1991 Jan 28; 28(1):6-9. PubMed ID: 1999837
    [Abstract] [Full Text] [Related]

  • 20. Sex chromosome marker: clinical significance and DNA characterization.
    Johnson VP, McDonough PG, Cheung SW, Sun L.
    Am J Med Genet; 1991 Apr 01; 39(1):97-101. PubMed ID: 1867271
    [Abstract] [Full Text] [Related]

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