BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

301 related articles for article (PubMed ID: 12210351)

  • 1. 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]  

  • 2. Unique (Y;13) translocation in a male with oligozoospermia: cytogenetic and molecular studies.
    Alves C; Carvalho F; Cremades N; Sousa M; Barros A
    Eur J Hum Genet; 2002 Aug; 10(8):467-74. PubMed ID: 12111641
    [TBL] [Abstract][Full Text] [Related]  

  • 3. Detection of t(X;Y) in 2 XX males using fluorescent in situ hybridization.
    Taiar N; Qumsiyeh MB; Croteau S; Rollet J; Benkhalifa M
    Ann Genet; 1995; 38(2):102-5. PubMed ID: 7486824
    [TBL] [Abstract][Full Text] [Related]  

  • 4. Cytogenetic, molecular and testicular tissue studies in an infertile 45,X male carrying an unbalanced (Y;22) translocation: case report.
    Brisset S; Izard V; Misrahi M; Aboura A; Madoux S; Ferlicot S; Schoevaert D; Soufir JC; Frydman R; Tachdjian G
    Hum Reprod; 2005 Aug; 20(8):2168-72. PubMed ID: 15845593
    [TBL] [Abstract][Full Text] [Related]  

  • 5. A Y/15 translocation in a 45,X male with Prader-Willi syndrome.
    Puvabanditsin S; Garrow E; Razi S; Mohar AG; Tadros JJ; Phattraprayoon N; Patel P
    Genet Couns; 2007; 18(4):417-21. PubMed ID: 18286823
    [TBL] [Abstract][Full Text] [Related]  

  • 6. Familial whole-arm translocations (1;19), (9;13), and (12;21): a review of 101 constitutional exchanges.
    Vázquez-Cárdenas A; Vásquez-Velásquez AI; Barros-Núñez P; Mantilla-Capacho J; Rocchi M; Rivera H
    J Appl Genet; 2007; 48(3):261-8. PubMed ID: 17666779
    [TBL] [Abstract][Full Text] [Related]  

  • 7. Prenatal diagnosis of a 45,X male with a SRY-bearing chromosome 21.
    Nataf V; Senat MV; Albert M; Bidat L; de Mazancourt P; Roume J; Allard L; Le Tessier D; Ville Y; Selva J
    Prenat Diagn; 2002 Aug; 22(8):675-80. PubMed ID: 12210575
    [TBL] [Abstract][Full Text] [Related]  

  • 8. 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]  

  • 9. Unique t(Y;1)(q12;q12) reciprocal translocation with loss of the heterochromatic region of chromosome 1 in a male with azoospermia due to meiotic arrest: a case report.
    Pinho MJ; Neves R; Costa P; Ferrás C; Sousa M; Alves C; Almeida C; Fernandes S; Silva J; Ferrás L; Barros A
    Hum Reprod; 2005 Mar; 20(3):689-96. PubMed ID: 15665019
    [TBL] [Abstract][Full Text] [Related]  

  • 10. The use of fluorescence in-situ hybridisation to clarify abnormal Y chromosomes in two infertile men.
    Smith A; Conway A; Robson L
    Med J Aust; 1994 May; 160(9):545, 548-9, 552. PubMed ID: 8164552
    [TBL] [Abstract][Full Text] [Related]  

  • 11. 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]  

  • 12. Molecular and cytogenetic characterization of a structural rearrangement of the Y chromosome in an azoospermic man.
    Valetto A; Bertini V; Rapalini E; Baldinotti F; Di Martino D; Simi P
    Fertil Steril; 2004 May; 81(5):1388-90. PubMed ID: 15136108
    [TBL] [Abstract][Full Text] [Related]  

  • 13. Characterization of the first adult de novo case of 46,X,der(Y)t(X;Y)(p22.3;q11.2).
    Bukvic N; Cesarano C; Ceccarini C; Bruno M; Lipsi MR; Gallicchio MG; Carboni MA; Valente L; Cotoia G; Antonetti R
    Gene; 2013 Jan; 513(1):111-7. PubMed ID: 23124038
    [TBL] [Abstract][Full Text] [Related]  

  • 14. An azoospermic male with an unbalanced autosomal-Y translocation.
    Yoshida A; Nakahori Y; Kuroki Y; Miura K; Shirai M
    Jpn J Hum Genet; 1997 Sep; 42(3):451-5. PubMed ID: 12503194
    [TBL] [Abstract][Full Text] [Related]  

  • 15. Infertility in a man with oligoasthenoteratozoospermia associated with nonrobertsonian translocation t(9;15)(p10;q10).
    Aydos SE; Tükün A
    Fertil Steril; 2006 Oct; 86(4):1001.e7-9. PubMed ID: 17027368
    [TBL] [Abstract][Full Text] [Related]  

  • 16. 47,X,idic(Y),inv dup(Y): a non-mosaic case of a phenotypically normal boy with two different Y isochromosomes and neocentromere formation.
    Pasantes JJ; Wimmer R; Knebel S; Münch C; Kelbova C; Junge A; Kieback P; Küpferling P; Schempp W
    Cytogenet Genome Res; 2012; 136(2):157-62. PubMed ID: 22286088
    [TBL] [Abstract][Full Text] [Related]  

  • 17. A dysmorphic newborn with 45,X,der(1)inv(1)(p13;qter)t(Y;1)(pter-->q11;p13),-Y de novo karyotype.
    Tatar A; Oztas S; Yakut T; Ors R
    Genet Couns; 2005; 16(2):173-7. PubMed ID: 16080298
    [TBL] [Abstract][Full Text] [Related]  

  • 18. Crypt Y chromosome fragment resulting from an X;Y translocation in a patient with premature ovarian failure.
    Cheng DH; Tan YQ; Di YF; Li LY; Lu GX
    Fertil Steril; 2009 Aug; 92(2):828.e3-6. PubMed ID: 19524892
    [TBL] [Abstract][Full Text] [Related]  

  • 19. 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]  

  • 20. An infertile male with apparent 45,X turned out to have 45,X,der(Y)t(Y;13)(q11.2;q12),-13: clinicopathologic and cytogenomic studies.
    Cui YX; Xia XY; Pan LJ; Wang YH; Yao B; Huang YF
    Fertil Steril; 2007 Dec; 88(6):1676.e7-11. PubMed ID: 17482602
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 16.