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Journal Abstract Search

291 related items for PubMed ID: 8488881

  • 1. 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
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  • 3. 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
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  • 6. 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 Jan 15; 28(4):214-8. PubMed ID: 3879431
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  • 7. 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 02; 160(9):545, 548-9, 552. PubMed ID: 8164552
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  • 8. 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 02; 20(8):2168-72. PubMed ID: 15845593
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  • 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 02; 20(3):689-96. PubMed ID: 15665019
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  • 10. Translocation 46,X,t(Y;14)(q122;q111) in a case of sterility in the male.
    Petit P, Unglik A, Fryns JP.
    Ann Genet; 1982 Mar 02; 25(1):63-4. PubMed ID: 6979304
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  • 11. 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 Mar 02; 19(3):277-80. PubMed ID: 18990982
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  • 12. Infertility in a man with oligoasthenoteratozoospermia associated with nonrobertsonian translocation t(9;15)(p10;q10).
    Aydos SE, Tükün A.
    Fertil Steril; 2006 Oct 02; 86(4):1001.e7-9. PubMed ID: 17027368
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  • 13. 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 Oct 02; 39(1):10-5. PubMed ID: 9297438
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  • 14. 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 Oct 02; 12(1):95-100. PubMed ID: 11332984
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  • 16. Severe oligospermia associated with a unique balanced reciprocal translocation t(6;12)(q23;q24.3): male infertility related to t(6;12).
    Bianco B, Christofolini D, Gava M, Mafra F, Moraes E, Barbosa C.
    Andrologia; 2011 Apr 02; 43(2):145-8. PubMed ID: 21382069
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  • 17. [Chromosome anomalies in human azoospermia].
    Sozanskiĭ OA, Guleniuk NL, Akopian GR, Zabrodskiĭ BT.
    Genetika; 1988 Jul 02; 24(7):1299-303. PubMed ID: 3181753
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  • 18. Reciprocal translocation t(7;16)(q21.2;p13.3) in an infertile man.
    Mikelsaar R, Pauklin M, Lissitsina J, Punab M.
    Fertil Steril; 2006 Sep 02; 86(3):719.e9-11. PubMed ID: 16952514
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  • 19. 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 02; 10(8):467-74. PubMed ID: 12111641
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  • 20. [Translocation 46,X, t(Y;7)(q122;q11) in a case of male sterility].
    Turleau C, Croquette MF, Fourlinnie JC, Desmons F, Grouchy J.
    Ann Genet; 1976 Sep 02; 19(3):210-2. PubMed ID: 1086632
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