BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

116 related articles for article (PubMed ID: 3228133)

  • 1. Two mosaic cases with nonfluorescent Y chromosome analysed with Y-specific DNA probes.
    Kałuzewski B; Jakubowski L; Debiec-Rychter M; Grzeschik KH; Limon J; Gibas Z
    Am J Med Genet; 1988 Nov; 31(3):489-503. PubMed ID: 3228133
    [TBL] [Abstract][Full Text] [Related]  

  • 2. Phenotype/karyotype correlations of Y chromosome aneuploidy with emphasis on structural aberrations in postnatally diagnosed cases.
    Hsu LY
    Am J Med Genet; 1994 Nov; 53(2):108-40. PubMed ID: 7856637
    [TBL] [Abstract][Full Text] [Related]  

  • 3. Clinical consequences of a human non-fluorescent Y chromosome (Ynf).
    Sahdev S; Verma RS; Macera MJ; Vohra K; Jhaveri RC; Flores R
    Ann Genet; 1989; 32(4):241-3. PubMed ID: 2610491
    [TBL] [Abstract][Full Text] [Related]  

  • 4. [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]  

  • 5. A theory explaining the abnormality in 45,X/46,XY mosaicism with non-fluorescent Y chromosome. presentation of three cases.
    Kaluzewski B; Jokinen A; Hortling H; de la Chapelle A
    Ann Genet; 1978 Mar; 21(1):5-11. PubMed ID: 308343
    [TBL] [Abstract][Full Text] [Related]  

  • 6. [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]  

  • 7. [Identification of Y chromosome material in an XX male by means of fluorescent in situ hybridization].
    Brandt CA; Hindkjaer J; Strømkjaer H; Christensen MF; Kølvraa S
    Ugeskr Laeger; 1992 Nov; 154(47):3321-4. PubMed ID: 1462437
    [TBL] [Abstract][Full Text] [Related]  

  • 8. Application of fluorescent in situ hybridization with X and Y chromosome specific probes to buccal smear analysis.
    Schad CR; Kuffel DG; Wyatt WA; Zinsmeister AR; Jenkins RB; Dewald GW; Jalal SM
    Am J Med Genet; 1996 Dec; 66(2):187-92. PubMed ID: 8958328
    [TBL] [Abstract][Full Text] [Related]  

  • 9. Cytogenetic and molecular investigations of an abnormal Y chromosome: evidence for a pseudo-dicentric (Yq) isochromosome.
    Savary JB; Vasseur F; Flactif M; Willatt L; Lefebvre J; Ferguson-Smith MA; Deminatti MM
    Ann Genet; 1992; 35(3):134-9. PubMed ID: 1466561
    [TBL] [Abstract][Full Text] [Related]  

  • 10. Mapping of testis-determining locus on Yp by the molecular genetic analysis of XX males and XY females.
    Müller U
    Development; 1987; 101 Suppl():51-8. PubMed ID: 3503723
    [TBL] [Abstract][Full Text] [Related]  

  • 11. 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]  

  • 12. 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]  

  • 13. Presence of Y chromosome sequences and their effect on the phenotype of six patients with Y chromosome anomalies.
    Shankman S; Spurdle AB; Morris D; Rosendorff J; Marques I; Bernstein R; Ramsay M
    Am J Med Genet; 1995 Jan; 55(3):269-75. PubMed ID: 7726221
    [TBL] [Abstract][Full Text] [Related]  

  • 14. Y-specific DNA sequences in male patients with 46,XX and 47,XXX karyotypes.
    Müller U; Latt SA; Donlon T
    Am J Med Genet; 1987 Oct; 28(2):393-401. PubMed ID: 2827475
    [TBL] [Abstract][Full Text] [Related]  

  • 15. Highly homologous loci on the X and Y chromosomes are hot-spots for ectopic recombinations leading to XX maleness.
    Weil D; Wang I; Dietrich A; Poustka A; Weissenbach J; Petit C
    Nat Genet; 1994 Jul; 7(3):414-9. PubMed ID: 7920661
    [TBL] [Abstract][Full Text] [Related]  

  • 16. [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]  

  • 17. Identification of ring Y chromosome: cytogenetic analysis, Southern blot and fluorescent in situ hybridization.
    Pezzolo A; Perroni L; Gimelli G; Arslanian A; Porta S; Gandullia P; Gandullia E
    Ann Genet; 1993; 36(2):121-5. PubMed ID: 8215218
    [TBL] [Abstract][Full Text] [Related]  

  • 18. Phenotypic variability in isodicentric Y patients: study of nine cases.
    DesGroseilliers M; Beaulieu Bergeron M; Brochu P; Lemyre E; Lemieux N
    Clin Genet; 2006 Aug; 70(2):145-50. PubMed ID: 16879197
    [TBL] [Abstract][Full Text] [Related]  

  • 19. Turner syndrome: a cytogenetic and molecular study.
    Jacobs P; Dalton P; James R; Mosse K; Power M; Robinson D; Skuse D
    Ann Hum Genet; 1997 Nov; 61(Pt 6):471-83. PubMed ID: 9543547
    [TBL] [Abstract][Full Text] [Related]  

  • 20. [Molecular analysis of the Y chromosome in XX sex-reversed patients].
    Chernykh VB; Chukhrova AL; Vasserman NN; Il'ina EV; Karmanov ME; Fedotov VP; Poliakov AV
    Genetika; 2008 Feb; 44(2):236-41. PubMed ID: 18619043
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 6.