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Pubmed for Handhelds

PUBMED FOR HANDHELDS

Journal Abstract Search

192 related items for PubMed ID: 3491577

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  • 3. Meiotic segregation analysis in spermatozoa of pericentric inversion carriers using fluorescence in-situ hybridization.
    Morel F, Laudier B, Guérif F, Couet ML, Royère D, Roux C, Bresson JL, Amice V, De Braekeleer M, Douet-Guilbert N.
    Hum Reprod; 2007 Jan; 22(1):136-41. PubMed ID: 16917123
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  • 4. Synaptonemal complexes in a subfertile man with a pericentric inversion in chromosome 21. Heterosynapsis without previous homosynapsis.
    Gabriel-Robez O, Ratomponirina C, Croquette M, Couturier J, Rumpler Y.
    Cytogenet Cell Genet; 1988 Jan; 48(2):84-7. PubMed ID: 3197453
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  • 6. Synapsis of a chromosomal pair heterozygous for a pericentric inversion and the presence of a heterochromatic short arm.
    Hale DW, Greenbaum IF.
    Cytogenet Cell Genet; 1988 Jan; 48(1):55-7. PubMed ID: 3180849
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  • 8. [Familial pericentric inversion of chromosome 10. 2 new cases].
    Teyssier M, Moreau N.
    Ann Genet; 1983 Jan; 26(3):183-6. PubMed ID: 6606382
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  • 10. TEM, FISH and molecular studies in infertile men with pericentric inversion of chromosome 9.
    Collodel G, Moretti E, Capitani S, Piomboni P, Anichini C, Estenoz M, Baccetti B.
    Andrologia; 2006 Aug; 38(4):122-7. PubMed ID: 16872463
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  • 11. Heterosynapsis and suppression of chiasmata within heterozygous pericentric inversions of the Sitka deer mouse.
    Hale DW.
    Chromosoma; 1986 Aug; 94(6):425-32. PubMed ID: 3829831
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  • 14. Pericentric inversion in human chromosome 1 and the risk for male sterility.
    Chandley AC, McBeath S, Speed RM, Yorston L, Hargreave TB.
    J Med Genet; 1987 Jun; 24(6):325-34. PubMed ID: 3612704
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  • 17. Familial pericentric inversion of chromosome 1 (p34q23) and male infertility with stage specific spermatogenic arrest.
    Meschede D, Froster UG, Bergmann M, Nieschlag E.
    J Med Genet; 1994 Jul; 31(7):573-5. PubMed ID: 7966196
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  • 18. Synaptonemal complex karyotyping in an oligospermic patient with heterochromatin duplication in chromosome n. 9.
    Solari AJ, Ponzio R, Rey Valzacchi G.
    Medicina (B Aires); 1991 Jul; 51(3):217-21. PubMed ID: 1821904
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  • 20. The meiotic pairing behaviour in human spermatocytes carrier of chromosome anomalies and their repercussions on reproductive fitness. I: Inversions and insertions. A European collaborative study.
    Gabriel-Robez O, Rumpler Y.
    Ann Genet; 1994 Jul; 37(1):3-10. PubMed ID: 8010710
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