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.


BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

233 related articles for article (PubMed ID: 8966091)

  • 1. [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; 71(3):203-9. PubMed ID: 8966091
    [TBL] [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; 42(5):720-3. PubMed ID: 1632446
    [TBL] [Abstract][Full Text] [Related]  

  • 3. [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; 47(2):117-25. PubMed ID: 7610280
    [TBL] [Abstract][Full Text] [Related]  

  • 4. [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; 26(4):461-4. PubMed ID: 20017317
    [TBL] [Abstract][Full Text] [Related]  

  • 5. [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; 42(10):679-82. PubMed ID: 18241543
    [TBL] [Abstract][Full Text] [Related]  

  • 6. [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
    [TBL] [Abstract][Full Text] [Related]  

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

  • 8. [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; 26(6):659-63. PubMed ID: 19953489
    [TBL] [Abstract][Full Text] [Related]  

  • 9. 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
    [TBL] [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; 15(2):89-100. PubMed ID: 15524154
    [TBL] [Abstract][Full Text] [Related]  

  • 11. 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; 56(2):141-6. PubMed ID: 7625435
    [TBL] [Abstract][Full Text] [Related]  

  • 12. 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; 150(1):70-2. PubMed ID: 15041227
    [TBL] [Abstract][Full Text] [Related]  

  • 13. [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
    [TBL] [Abstract][Full Text] [Related]  

  • 14. 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
    [TBL] [Abstract][Full Text] [Related]  

  • 15. 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; 37(1):71-8. PubMed ID: 2240047
    [TBL] [Abstract][Full Text] [Related]  

  • 16. [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
    [TBL] [Abstract][Full Text] [Related]  

  • 17. Paternally derived der(7)t(Y;7)(p11.1 approximately 11.2;p22.3)dn in a mosaic case with Turner syndrome.
    Polityko AD; Khurs OM; Kulpanovich AI; Mosse KA; Solntsava AV; Rumyantseva NV; Naumchik IV; Liehr T; Weise A; Mkrtchyan H
    Eur J Med Genet; 2009; 52(4):207-10. PubMed ID: 19375526
    [TBL] [Abstract][Full Text] [Related]  

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

  • 19. Gonadoblastoma in patients with Ullrich-Turner syndrome.
    Zelaya G; López Marti JM; Marino R; Garcia de Dávila MT; Gallego MS
    Pediatr Dev Pathol; 2015; 18(2):117-21. PubMed ID: 25535833
    [TBL] [Abstract][Full Text] [Related]  

  • 20. Identification of marker chromosomes in thirteen patients using FISH probing.
    Daniel A; Malafiej P; Preece K; Chia N; Nelson J; Smith M
    Am J Med Genet; 1994 Oct; 53(1):8-18. PubMed ID: 7802042
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 12.