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Journal Abstract Search

423 related items for PubMed ID: 15333598

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  • 3. Molecular analysis of the IVS8-T splice variant 5T and M470V exon 10 missense polymorphism in Iranian males with congenital bilateral absence of the vas deferens.
    Radpour R, Gilani MA, Gourabi H, Dizaj AV, Mollamohamadi S.
    Mol Hum Reprod; 2006 Jul; 12(7):469-73. PubMed ID: 16714368
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  • 4. 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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  • 5. Improved detection of cystic fibrosis mutations in infertility patients with DNA sequence analysis.
    Danziger KL, Black LD, Keiles SB, Kammesheidt A, Turek PJ.
    Hum Reprod; 2004 Mar 01; 19(3):540-6. PubMed ID: 14998948
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  • 6. Two novel missense and one novel nonsense CFTR mutations in Iranian males with congenital bilateral absence of the vas deferens.
    Radpour R, Gourabi H, Gilani MA, Dizaj AV, Rezaee M, Mollamohamadi S.
    Mol Hum Reprod; 2006 Nov 01; 12(11):717-21. PubMed ID: 16973827
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  • 7. 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 Nov 01; 64(3):213-8. PubMed ID: 15239534
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  • 8. Mutations of the CFTR gene in Turkish patients with congenital bilateral absence of the vas deferens.
    Dayangaç D, Erdem H, Yilmaz E, Sahin A, Sohn C, Ozgüç M, Dörk T.
    Hum Reprod; 2004 May 01; 19(5):1094-100. PubMed ID: 15070876
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  • 9. Spectrum of CFTR mutations in cystic fibrosis and in congenital absence of the vas deferens in France.
    Claustres M, Guittard C, Bozon D, Chevalier F, Verlingue C, Ferec C, Girodon E, Cazeneuve C, Bienvenu T, Lalau G, Dumur V, Feldmann D, Bieth E, Blayau M, Clavel C, Creveaux I, Malinge MC, Monnier N, Malzac P, Mittre H, Chomel JC, Bonnefont JP, Iron A, Chery M, Georges MD.
    Hum Mutat; 2000 May 01; 16(2):143-56. PubMed ID: 10923036
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  • 10. A novel missense mutation P1290S at exon-20 of the CFTR gene in a Portuguese patient with congenital bilateral absence of the vas deferens.
    Grangeia A, Carvalho F, Fernandes S, Silva J, Sousa M, Barros A.
    Fertil Steril; 2005 Feb 01; 83(2):448-51. PubMed ID: 15705389
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  • 11. Molecular diagnosis of congenital bilateral absence of the vas deferens: analyses of the CFTR gene in 64 French patients.
    Bienvenu T, Adjiman M, Thiounn N, Jeanpierre M, Hubert D, Lepercoq J, Francoual C, Wolf J, Izard V, Jouannet P, Kaplan JC, Beldjord C.
    Ann Genet; 1997 Feb 01; 40(1):5-9. PubMed ID: 9150843
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  • 12. Molecular study of (TG)m(T)n polymorphisms in Iranian males with congenital bilateral absence of the vas deferens.
    Radpour R, Gourabi H, Gilani MA, Dizaj AV.
    J Androl; 2007 Feb 01; 28(4):541-7. PubMed ID: 17314234
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  • 13. CFTR (TG)m(T)n polymorphism in patients with CBAVD in a population expressing low incidence of cystic fibrosis.
    Chiang HS, Lu JF, Liu CH, Wu YN, Wu CC.
    Clin Genet; 2009 Sep 01; 76(3):282-6. PubMed ID: 19737283
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  • 16. Clinical, andrological and genetic characteristics of patients with congenital bilateral absence of vas deferens (CBAVD).
    Samli H, Samli MM, Yilmaz E, Imirzalioglu N.
    Arch Androl; 2006 Sep 01; 52(6):471-7. PubMed ID: 17050329
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  • 17. CFTR mutations and polymorphisms in male infertility.
    Cuppens H, Cassiman JJ.
    Int J Androl; 2004 Oct 01; 27(5):251-6. PubMed ID: 15379964
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