BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

187 related articles for article (PubMed ID: 12439894)

  • 21. Structural analysis of a rare rearranged Y chromosome and its bearing on genotype-phenotype correlation.
    Ogata T; Wakui K; Kosho T; Muroya K; Yamanouchi Y; Takano T; Fukushima Y; Rappold G; Suzuki Y
    Am J Med Genet; 2000 Jun; 92(4):256-9. PubMed ID: 10842291
    [TBL] [Abstract][Full Text] [Related]  

  • 22. Clinical and molecular cytogenetic studies in three infertile patients with mosaic rearranged Y chromosomes.
    Bettio D; Venci A; Rizzi N; Negri L; Setti PL
    Hum Reprod; 2006 Apr; 21(4):972-5. PubMed ID: 16484313
    [TBL] [Abstract][Full Text] [Related]  

  • 23. [Cytogenetic and molecular genetic analysis of a case with mosaic marker chromosomes].
    Tu X; Zeng J; Cong X; Zhang X; Yan A
    Zhonghua Yi Xue Yi Chuan Xue Za Zhi; 2016 Feb; 33(1):76-80. PubMed ID: 26829740
    [TBL] [Abstract][Full Text] [Related]  

  • 24. 47,XX + mar karyotype containing genes from the azoospermia factor region. A case report.
    Causio F; Gentile E; Fischetto R; Archidiacono N; Magro N
    J Reprod Med; 2002 Jul; 47(7):575-80. PubMed ID: 12170536
    [TBL] [Abstract][Full Text] [Related]  

  • 25. [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]  

  • 26. Alphoidless centromere of a familial unstable inverted Y chromosome.
    Rivera H; Vassquez AI; Ayala-Madrigal ML; Ramirez-Dueñas ML; Davalos IP
    Ann Genet; 1996; 39(4):236-9. PubMed ID: 9037351
    [TBL] [Abstract][Full Text] [Related]  

  • 27. Isodicentric Y (p11.32) chromosome in an infant with mixed gonadal dysgenesis.
    Aktas D; Alikasifoglu M; Gonc N; Senocak ME; Tuncbilek E
    Eur J Med Genet; 2006; 49(2):141-9. PubMed ID: 16530711
    [TBL] [Abstract][Full Text] [Related]  

  • 28. Mixed gonadal dysgenesis with 45,X/46,X,idic(Y)/46,XY,idic(Y) karyotype.
    Caglayan AO; Demiryilmaz F; Kendirci M; Ozyazgan I; Akalin H; Bittmann S
    Genet Couns; 2009; 20(2):173-9. PubMed ID: 19650415
    [TBL] [Abstract][Full Text] [Related]  

  • 29. Premature ovarian failure in a patient with a complex chromosome rearrangement involving the critical region Xq24, characterized by analysis using fluorescence in situ hybridization by chromosome microdissection.
    Weimer J; Shivakumar S; Danda S; Thomas N; Ralui LP; Jonat W; Arnold N
    Fertil Steril; 2007 Dec; 88(6):1677.e9-13. PubMed ID: 17482166
    [TBL] [Abstract][Full Text] [Related]  

  • 30. Molecular cytogenetic identification and characterization of a de novo supernumerary neocentromeric derivative chromosome 13.
    Tonnies H; Gerlach A; Heineking B; Starke H; Neitzel H; Neumann LM
    Cytogenet Genome Res; 2006; 114(3-4):325-9. PubMed ID: 16954674
    [TBL] [Abstract][Full Text] [Related]  

  • 31. Prenatal diagnosis of mos45,X/46,X,+mar in a fetus with normal male external genitalia and a literature review.
    Chien SC; Chen CP; Lin CC; Huang LC; Hsieh CT; Tsai FJ
    Taiwan J Obstet Gynecol; 2009 Sep; 48(3):292-5. PubMed ID: 19797023
    [TBL] [Abstract][Full Text] [Related]  

  • 32. [Sperm-fluorescence in situ hybridization analysis in patients with pericentric inversions of Y chromosome].
    Luo YQ; Qian YL; Lu HM; Xu CM; Jin F
    Zhonghua Yi Xue Yi Chuan Xue Za Zhi; 2009 Feb; 26(1):54-6. PubMed ID: 19199252
    [TBL] [Abstract][Full Text] [Related]  

  • 33. Characterization by fluorescence and electron microscopy in situ hybridization of a double Y isochromosome.
    Fetni R; Krabchi K; Messier PE; Richer CL; Lemieux N
    Am J Med Genet; 1996 Jun; 63(3):454-7. PubMed ID: 8737651
    [TBL] [Abstract][Full Text] [Related]  

  • 34. H-Y typing by ELISA in a 46,X,dic(Y)(q11.2101) male: effects of a nonmosaic Yp duplication.
    Moreira-Filho CA; Wachtel SS; Daniel A; Priest JH
    Am J Med Genet; 1987 Mar; 26(3):709-17. PubMed ID: 3565484
    [TBL] [Abstract][Full Text] [Related]  

  • 35. Centromeric association of a microchromosome Y in two male patients.
    Domínguez MG; Vásquez AI; Troyo R; Ortiz-Aranda M; Padilla JR; Hernández-Zaragoza G; Rivas F; Rivera H
    Genet Couns; 2006; 17(4):413-9. PubMed ID: 17375527
    [TBL] [Abstract][Full Text] [Related]  

  • 36. Fate of SRY, PABY, DYS1, DYZ3 and DYZ1 loci in Indian patients harbouring sex chromosomal anomalies.
    Bashamboo A; Rahman MM; Prasad A; Chandy SP; Ahmad J; Ali S
    Mol Hum Reprod; 2005 Feb; 11(2):117-27. PubMed ID: 15579656
    [TBL] [Abstract][Full Text] [Related]  

  • 37. Giemsa-11 technique elucidating three structurally altered nonfluorescent Y chromosomes: r (Y), idic (Yp), dir tan dup (Yp).
    Kosztolányi G
    Ann Genet; 1988; 31(4):235-40. PubMed ID: 3265307
    [TBL] [Abstract][Full Text] [Related]  

  • 38. Assessment of sex chromosome composition using fluorescent in situ hybridization as an adjunct to GTG-banding.
    Mark HF; Meyers-Seifer CH; Seifer DB; Demoranville BM; Jackson IM
    Ann Clin Lab Sci; 1995; 25(5):402-8. PubMed ID: 7486815
    [TBL] [Abstract][Full Text] [Related]  

  • 39. FISH and array CGH characterization of de novo derivative Y chromosome (Yq duplication and partial Yp deletion) in an azoospermic male.
    Wiland E; Yatsenko AN; Kishore A; Stanczak H; Zdarta A; Ligaj M; Olszewska M; Wolski JK; Kurpisz M
    Reprod Biomed Online; 2015 Aug; 31(2):217-24. PubMed ID: 26096031
    [TBL] [Abstract][Full Text] [Related]  

  • 40. First prenatally detected small supernumerary neocentromeric derivative chromosome 13 resulting in a non-mosaic partial tetrasomy 13q.
    Mascarenhas A; Matoso E; Saraiva J; Tönnies H; Gerlach A; Julião MJ; Melo JB; Carreira IM
    Cytogenet Genome Res; 2008; 121(3-4):293-7. PubMed ID: 18758175
    [TBL] [Abstract][Full Text] [Related]  

    [Previous]   [Next]    [New Search]
    of 10.