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 *

110 related articles for article (PubMed ID: 17375527)

  • 1. 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]  

  • 2. Isodicentric Y chromosomes and secondary microchromosomes.
    Rivera H; Ayala-Madrigal LM; Gutiérrez-Angulo M; Vasquez AI; Ramos AL
    Genet Couns; 2003; 14(2):227-31. PubMed ID: 12872818
    [TBL] [Abstract][Full Text] [Related]  

  • 3. A 45,X sterile male with Yp disguised as 21p.
    Dávalos IP; Rivera H; Vásquez AI; Gutiérrez-Angulo M; Hernández-Vázquez MC; Cortina-Luna FA; Wong-Ley LE; Domínguez-Quezada MG
    Am J Med Genet; 2002 Aug; 111(2):202-4. PubMed ID: 12210351
    [TBL] [Abstract][Full Text] [Related]  

  • 4. [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]  

  • 5. [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]  

  • 6. Centromeric association of chromosome 16- and 18-derived microchromosomes.
    Felbor U; Rutschow D; Haaf T; Schmid M
    Hum Genet; 2002 Jul; 111(1):16-25. PubMed ID: 12136231
    [TBL] [Abstract][Full Text] [Related]  

  • 7. Centromeric association of a microchromosome in a Turner syndrome patient with a pseudodicentric Y.
    Rivera H; Domínguez MG; Vásquez AI; Ramos AL; Fragoso R
    Hum Genet; 1993 Nov; 92(5):522-4. PubMed ID: 8244347
    [TBL] [Abstract][Full Text] [Related]  

  • 8. [Y chromosome structural abnormalities and Turner's syndrome].
    Ravel C; Siffroi JP
    Gynecol Obstet Fertil; 2009 Jun; 37(6):511-8. PubMed ID: 19464936
    [TBL] [Abstract][Full Text] [Related]  

  • 9. [GH deficiency in a male patient with 45 X0 karyotype and Yp/18p- translocation. Report of a case].
    Sposito M; Bingener A; Mizzoni F; Farinelli E; Vaccaro R
    Minerva Pediatr; 2003 Oct; 55(5 Suppl 1):79-81. PubMed ID: 14992190
    [No Abstract]   [Full Text] [Related]  

  • 10. [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]  

  • 11. Identification of a neocentromere in a rearranged Y chromosome with no detectable DYZ3 centromeric sequence.
    Assumpção JG; Berkofsky-Fessler W; Viguetti Campos N; Trevas Maciel-Guerra A; Li S; Melaragno MI; Palandi de Mello M; Warburton PE
    Am J Med Genet; 2002 Dec; 113(3):263-7. PubMed ID: 12439894
    [TBL] [Abstract][Full Text] [Related]  

  • 12. Pseudodicentric 22;Y translocation transmitted through four generations of a large family without phenotypic repercussion.
    Morales C; Soler A; Bruguera J; Madrigal I; Alsius M; Obon M; Margarit E; Sánchez A
    Cytogenet Genome Res; 2007; 116(4):319-23. PubMed ID: 17431332
    [TBL] [Abstract][Full Text] [Related]  

  • 13. [Dicentric Yp chromosome as one of the reasons for the absence of fluorescence in human Y chromosome].
    Verlinskaia DK; Prozorova MV
    Tsitologiia; 1983 Jun; 25(6):696-8. PubMed ID: 6684338
    [TBL] [Abstract][Full Text] [Related]  

  • 14. Dynamic increase of a 45,X cell line in a patient with multicentric ring Y chromosomes.
    DesGroseilliers M; Fortin F; Lafrenière AM; Brochu P; Lemyre E; Lemieux N
    Cytogenet Genome Res; 2006; 115(1):90-3. PubMed ID: 16974088
    [TBL] [Abstract][Full Text] [Related]  

  • 15. Ambiguous genitalia by 9p deletion inherent to a dic(Y;9)(q12;p24).
    Vásquez-Velásquez AI; Arnaud-López L; Figuera LE; Padilla-Gutiérrez JR; Rivas F; Rivera H
    J Appl Genet; 2005; 46(4):415-8. PubMed ID: 16278517
    [TBL] [Abstract][Full Text] [Related]  

  • 16. A further microchromosome with centromeric association.
    Rivera H; Dominguez MG; Vasquez AI; Mejia-Baltodano G
    Genet Couns; 1997; 8(4):323-6. PubMed ID: 9457502
    [TBL] [Abstract][Full Text] [Related]  

  • 17. Y chromosome heterochromatin of differing lengths in two cell populations of the same individual.
    Akkari Y; Lawce H; Kelson S; Smith C; Davis C; Boyd L; Magenis RE; Olson S
    Prenat Diagn; 2005 Apr; 25(4):304-6. PubMed ID: 15849801
    [TBL] [Abstract][Full Text] [Related]  

  • 18. OCT4 gonadal gene expression related to the presence of Y-chromosome sequences in Turner syndrome.
    Bianco B; Oliveira KC; Guedes AD; Barbosa CP; Lipay MV; Verreschi IT
    Fertil Steril; 2010 Nov; 94(6):2347-9. PubMed ID: 20347080
    [TBL] [Abstract][Full Text] [Related]  

  • 19. Preimplantation genetic screening (PGS) in infertile female age > or = 35 years by fluorescence in situ hybridization of chromosome 13, 18, 21, X and Y.
    Chiamchanya C; Visutakul P; Gumnarai N; Su-angkawatin W
    J Med Assoc Thai; 2008 Nov; 91(11):1644-50. PubMed ID: 19127783
    [TBL] [Abstract][Full Text] [Related]  

  • 20. Familial supernumerary microchromosome mosaicism: phenotypic effects and an attempt at characterization.
    Chudley AE; Zheng HZ; Pabello PD; Shia G; Wang HC
    Am J Med Genet; 1983 Sep; 16(1):89-97. PubMed ID: 6195920
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 6.