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PUBMED FOR HANDHELDS

Journal Abstract Search

452 related items for PubMed ID: 17329263

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  • 7. CFTR mutations and polymorphisms in male infertility.
    Cuppens H, Cassiman JJ.
    Int J Androl; 2004 Oct; 27(5):251-6. PubMed ID: 15379964
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  • 8. Analysis of the CFTR gene in Iranian cystic fibrosis patients: identification of eight novel mutations.
    Alibakhshi R, Kianishirazi R, Cassiman JJ, Zamani M, Cuppens H.
    J Cyst Fibros; 2008 Mar; 7(2):102-9. PubMed ID: 17662673
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  • 12. Congenital absence of vas deferens and cystic fibrosis.
    Leonardi S, Bombace V, Rotolo N, Sciuto C, La Rosa M.
    Minerva Pediatr; 2003 Feb; 55(1):43-7, 47-50. PubMed ID: 12660625
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  • 15. [Molecular basis of cystic fibrosis and congenital bilateral agenesis of vas deferens].
    Bienvenu T, Claustres M.
    Contracept Fertil Sex; 1996 Jun; 24(6):495-500. PubMed ID: 8766513
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  • 16. Mutations in CFTR gene and clinical correlation in Argentine patients with congenital bilateral absence of the vas deferens.
    Levy EM, Granados P, Rawe V, Olmedo SB, Luna MC, Cafferata E, Pivetta OH.
    Medicina (B Aires); 2004 Jun; 64(3):213-8. PubMed ID: 15239534
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  • 17. Characterization of cystic fibrosis conductance transmembrane regulator gene mutations and IVS8 poly(T) variants in Portuguese patients with congenital absence of the vas deferens.
    Grangeia A, Niel F, Carvalho F, Fernandes S, Ardalan A, Girodon E, Silva J, Ferrás L, Sousa M, Barros A.
    Hum Reprod; 2004 Nov; 19(11):2502-8. PubMed ID: 15333598
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  • 18. Mutations in the cystic fibrosis gene in patients with congenital absence of the vas deferens.
    Chillón M, Casals T, Mercier B, Bassas L, Lissens W, Silber S, Romey MC, Ruiz-Romero J, Verlingue C, Claustres M.
    N Engl J Med; 1995 Jun 01; 332(22):1475-80. PubMed ID: 7739684
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