BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

256 related articles for article (PubMed ID: 1632446)

  • 1. 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]  

  • 2. 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]  

  • 3. [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]  

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

  • 5. [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]  

  • 6. 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]  

  • 7. Mental retardation and Ullrich-Turner syndrome in cases with 45,X/46X,+mar: additional support for the loss of the X-inactivation center hypothesis.
    Cole H; Huang B; Salbert BA; Brown J; Howard-Peebles PN; Black SH; Dorfmann A; Febles OR; Stevens CA; Jackson-Cook C
    Am J Med Genet; 1994 Aug; 52(2):136-45. PubMed ID: 7801998
    [TBL] [Abstract][Full Text] [Related]  

  • 8. [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]  

  • 9. [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]  

  • 10. [Molecular detection of chromosome Y DNA sequences in patients with Turner's syndrome].
    López López M; Torres Maldonado LC; Pablo Méndez J; Cervantes Peredo A; Canto Cetina P; Pérez-Palacios G; Kofman-Alfaro S
    Rev Invest Clin; 1993; 45(3):233-9. PubMed ID: 8210766
    [TBL] [Abstract][Full Text] [Related]  

  • 11. [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]  

  • 12. 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]  

  • 13. PCR-based study of the presence of Y-chromosome sequences in patients with Ullrich-Turner syndrome.
    Coto E; Toral JF; Menéndez MJ; Hernando I; Plasencia A; Benavides A; López-Larrea C
    Am J Med Genet; 1995 Jul; 57(3):393-6. PubMed ID: 7677140
    [TBL] [Abstract][Full Text] [Related]  

  • 14. [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]  

  • 15. Novel ring chromosome composed of X- and Y-derived material in a girl with manifestations of Ullrich-Turner syndrome.
    Grass FS; Brown CA; Backeljauw PF; Lucas A; Brasington C; Gazak JM; Nakano S; Ostrowski RS; Spence JE
    Am J Med Genet; 2000 Aug; 93(5):343-8. PubMed ID: 10951455
    [TBL] [Abstract][Full Text] [Related]  

  • 16. 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; 50(3):251-4. PubMed ID: 8042669
    [TBL] [Abstract][Full Text] [Related]  

  • 17. [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]  

  • 18. 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; 18(4):393-9. PubMed ID: 18286820
    [TBL] [Abstract][Full Text] [Related]  

  • 19. 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]  

  • 20. A case with mosaic di-, tetra-, and octacentric ring Y chromosomes.
    Henegariu O; Pescovitz OH; Vance GH; Verbrugge J; Heerema NA
    Am J Med Genet; 1997 Sep; 71(4):426-9. PubMed ID: 9286449
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 13.