BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

166 related articles for article (PubMed ID: 23124038)

  • 1. 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]  

  • 2. Array-CGH characterization of a prenatally detected de novo 46,X,der(Y)t(X;Y)(p22.3;q11.2) in a male fetus.
    Palka C; Alfonsi M; Morizio E; Soranno A; La Rovere D; Matarrelli B; Rullo AL; Zori R; Chiarelli F; Calabrese G
    Eur J Med Genet; 2011; 54(3):333-6. PubMed ID: 21354345
    [TBL] [Abstract][Full Text] [Related]  

  • 3. Array-CGH characterization of a de novo t(X;Y)(p22;q11) in a female with short stature and mental retardation.
    Palka-Bayard-de-Volo C; De Marco S; Chiavaroli V; Alfonsi M; Calabrese G; Chiarelli F; Mohn A
    Gene; 2012 Aug; 504(1):107-10. PubMed ID: 22583828
    [TBL] [Abstract][Full Text] [Related]  

  • 4. Familial X;Y translocation with distinct phenotypic consequences: Characterization using FISH and array CGH.
    Bukvic N; Carri VD; Di Cosola ML; Pustorino G; Cesarano C; Chetta M; Santacroce R; Sarno M; Sessa F; Longo V; Novelli A; Gentile M; Margaglione M
    Am J Med Genet A; 2010 Jul; 152A(7):1730-4. PubMed ID: 20578256
    [TBL] [Abstract][Full Text] [Related]  

  • 5. Microphthalmia with linear skin defects (MLS) syndrome evaluated by prenatal karyotyping, FISH and array comparative genomic hybridization.
    Cain CC; Saul D; Attanasio L; Oehler E; Hamosh A; Blakemore K; Stetten G
    Prenat Diagn; 2007 Apr; 27(4):373-9. PubMed ID: 17286317
    [TBL] [Abstract][Full Text] [Related]  

  • 6. 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]  

  • 7. [Delineation of three structural Y chromosome aberrations combined molecular techniques].
    Tu XD; Zeng J; Cong XW; Yan AZ; Huang WJ; Lin YH; Zheng DZ; Zhang M; Wang ZH
    Zhonghua Yi Xue Yi Chuan Xue Za Zhi; 2013 Aug; 30(4):420-4. PubMed ID: 23926008
    [TBL] [Abstract][Full Text] [Related]  

  • 8. 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]  

  • 9. 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]  

  • 10. Prenatal diagnosis and prenatal imaging of a de novo 46,X,der(Y)t(X;Y)(p22.13;q11.23) leading to functional disomy for the distal end of the X chromosome short arm from Xp22.13 in a phenotypically male fetus with posterior fossa abnormalities.
    Ghosh A; Higgins L; Larkins SA; Miller C; Ostojic N; Martin WL; Kilby MD
    Prenat Diagn; 2008 Nov; 28(11):1068-71. PubMed ID: 18925617
    [No Abstract]   [Full Text] [Related]  

  • 11. 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]  

  • 12. Xp;Yq Unbalanced Translocation with Pseudoautosomal Region Aberrations in a Natural Two-Generation Transmission.
    Jiang Y; Yu Y; Zhang H; Zhang H; Sun M; Liu R
    Biomed Res Int; 2020; 2020():4976204. PubMed ID: 33344636
    [TBL] [Abstract][Full Text] [Related]  

  • 13. Characterization of a de novo unbalanced Y;autosome translocation in a 45,X mentally retarded male and literature review.
    Chen CP; Lin SP; Tsai FJ; Wang TH; Chern SR; Wang W
    Fertil Steril; 2008 Oct; 90(4):1198.e11-8. PubMed ID: 18304539
    [TBL] [Abstract][Full Text] [Related]  

  • 14. Prenatal diagnosis of sex chromosomal inversion, translocation and deletion.
    Zhang L; Ren M; Song G; Zhang Y; Liu X; Zhang X; Wang J
    Mol Med Rep; 2018 Feb; 17(2):2811-2816. PubMed ID: 29257243
    [TBL] [Abstract][Full Text] [Related]  

  • 15. [Prenatal diagnosis and genetic analysis of a fetus with der(X)t(X;Y)(p22.3;q11.2)].
    Li J; Dong Y; Li J; Luo J; Li C; Qi H
    Zhonghua Yi Xue Yi Chuan Xue Za Zhi; 2020 Nov; 37(11):1287-1290. PubMed ID: 33179242
    [TBL] [Abstract][Full Text] [Related]  

  • 16. Azoospermia and cryptorchidism in a male with a de novo reciprocal t(Y;16) translocation.
    Gunel M; Cavkaytar S; Ceylaner G; Batioglu S
    Genet Couns; 2008; 19(3):277-80. PubMed ID: 18990982
    [TBL] [Abstract][Full Text] [Related]  

  • 17. 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]  

  • 18. [Genetic study of a child carrying a maternally derived unbalanced 46,Y,der(X)t(X;Y)(p22;q11) chromosomal translocation].
    Yin T; Wang Y; Wang Z; Zhang R; Wang L
    Zhonghua Yi Xue Yi Chuan Xue Za Zhi; 2021 Apr; 38(4):376-379. PubMed ID: 33834470
    [TBL] [Abstract][Full Text] [Related]  

  • 19. Beckwith-Wiedemann syndrome due to 11p15.5 paternal duplication associated with Klinefelter syndrome and a "de novo" pericentric inversion of chromosome Y.
    Delicado A; Lapunzina P; Palomares M; Molina MA; Galán E; López Pajares I
    Eur J Med Genet; 2005; 48(2):159-66. PubMed ID: 16053907
    [TBL] [Abstract][Full Text] [Related]  

  • 20. Prenatal and postnatal characterization of Y chromosome structural anomalies by molecular cytogenetic analysis.
    Hernando C; Carrera M; Ribas I; Parear N; Baraibar R; Egocue J; Fuster C
    Prenat Diagn; 2002 Sep; 22(9):802-5. PubMed ID: 12224075
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 9.