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Journal Abstract Search

211 related items for PubMed ID: 2244061

  • 1.
    ; . PubMed ID:
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  • 2. [Translocation T (1;15) (Q21;P13) in a male with azoospermia].
    Antiñolo G, Borrego S, Fernández Vázquez L, Sánchez J.
    Actas Urol Esp; 1989; 13(6):465-6. PubMed ID: 2618838
    [Abstract] [Full Text] [Related]

  • 3. Case of (Y;1) familial translocation.
    Teyssier M, Rafat A, Pugeat M.
    Am J Med Genet; 1993 May 15; 46(3):339-40. PubMed ID: 8488881
    [Abstract] [Full Text] [Related]

  • 4. 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 15; 20(3):689-96. PubMed ID: 15665019
    [Abstract] [Full Text] [Related]

  • 5. 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 15; 42(3):451-5. PubMed ID: 12503194
    [Abstract] [Full Text] [Related]

  • 6. Characterization of a de novo t(Y;9) (q11.2;q22) by FISH technique.
    Conte RA, Kleyman SM, Klein V, Bialer MG, Verma RS.
    Ann Genet; 1996 Sep 15; 39(1):10-5. PubMed ID: 9297438
    [Abstract] [Full Text] [Related]

  • 7.
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  • 8. Chromosomal abnormalities in patients with azoospermia in Western Mexico.
    Meza-Espinoza JP, Davalos-Rodríguez IP, Rivera-Ramírez H, Perez-Muñoz S, Rivas-Solís F.
    Arch Androl; 2006 Sep 15; 52(2):87-90. PubMed ID: 16443583
    [Abstract] [Full Text] [Related]

  • 9. Translocation (Y;19)(q12;q13) and azoospermia.
    Diaz-Castaños LR, Rivera H, Gonzalez-Montes RM, Diaz M.
    Ann Genet; 1991 Sep 15; 34(1):27-9. PubMed ID: 1952788
    [Abstract] [Full Text] [Related]

  • 10. Aberrations of the synaptonemal complexes in a male 46,XY,-14,+der(14)t(Y;14).
    Ratomponirina C, Couturier J, Gabriel-Robez O, Rumpler Y, Dutrillaux B, Croquette M, Rabache Q, Leduc M.
    Ann Genet; 1985 Sep 15; 28(4):214-8. PubMed ID: 3879431
    [Abstract] [Full Text] [Related]

  • 11. 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 15; 20(8):2168-72. PubMed ID: 15845593
    [Abstract] [Full Text] [Related]

  • 12. A maternal inherited translocation t(1;22)(q11;p11) in two infertile brothers.
    Lorda-Sanchez I, Tejedor C, Sanz R, Rodriguez de Alba M, de la Fuente A, Fernandez E, Ayuso C, Ramos C.
    Genet Couns; 2001 Aug 15; 12(1):95-100. PubMed ID: 11332984
    [Abstract] [Full Text] [Related]

  • 13. [Chromosome anomalies in human azoospermia].
    Sozanskiĭ OA, Guleniuk NL, Akopian GR, Zabrodskiĭ BT.
    Genetika; 1988 Jul 15; 24(7):1299-303. PubMed ID: 3181753
    [Abstract] [Full Text] [Related]

  • 14. Segregation of chromosomes in sperm of a t(X;18)(q11;p11.1) carrier inherited from his mother: case report.
    Perrin A, Douet-Guilbert N, Le Bris MJ, Keromnes G, Langlois ML, Barrière P, Amice J, Amice V, De Braekeleer M, Morel F.
    Hum Reprod; 2008 Jan 15; 23(1):227-30. PubMed ID: 17986483
    [Abstract] [Full Text] [Related]

  • 15. 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 Jan 15; 38(2):102-5. PubMed ID: 7486824
    [Abstract] [Full Text] [Related]

  • 16. A 15p+ variant shown to be a t(Y;15) with fluorescence in situ hybridisation.
    Neumann AA, Robson LG, Smith A.
    Ann Genet; 1992 Jan 15; 35(4):227-30. PubMed ID: 1296520
    [Abstract] [Full Text] [Related]

  • 17. Azoospermic male with a balanced Y-autosome translocation.
    Matsuda T, Hayashi K, Nonomura M, Yamamoto S, Yoshida O.
    Urol Int; 1989 Jan 15; 44(1):43-6. PubMed ID: 2665261
    [Abstract] [Full Text] [Related]

  • 18. Mental retardation and Y/8 translocation [karyotype: 46,XY, t(Y;8)(q12;q24)] in father and son.
    Fryns JP, Kleczkowska A, Dereymaeker AM, Van den Berghe H.
    Helv Paediatr Acta; 1988 Aug 15; 43(1-2):87-90. PubMed ID: 3170249
    [Abstract] [Full Text] [Related]

  • 19. Characterization of a de novo balanced 1;Y translocation in a phenotypically normal twin male infant.
    Hatzissevastou-Loukidou H, Kalemi TG, Lambropoulos AF, Nikita M, Sotiridou E, Tarlatzis BC, Kotsis A.
    Fertil Steril; 2006 Apr 15; 85(4):1059.e5-7. PubMed ID: 16580398
    [Abstract] [Full Text] [Related]

  • 20. Preimplantation genetic diagnosis (PGD) for extremes--successful birth after PGD for a consanguineous couple carrying an identical balanced reciprocal translocation.
    Beyazyurek C, Ekmekci CG, Sağlam Y, Cinar C, Kahraman S.
    Fertil Steril; 2010 May 01; 93(7):2413.e1-5. PubMed ID: 20117768
    [Abstract] [Full Text] [Related]

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