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Journal Abstract Search

528 related items for PubMed ID: 16581722

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  • 2. Correlation between CFTR gene mutations in Iranian men with congenital absence of the vas deferens and anatomical genital phenotype.
    Radpour R, Gourabi H, Gilani MA, Dizaj AV.
    J Androl; 2008; 29(1):35-40. PubMed ID: 17673436
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  • 3. 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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  • 4. [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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  • 10. [Correlation of genitourinary abnormalities, spermiogram and CFTR genotype in patients with bilateral agenesis of the vas deferens].
    de la Taille A, Rigot JM, Mahe P, Gervais R, Dumur V, Lemaitre L, Mazeman E.
    Prog Urol; 1998 Jun; 8(3):370-6. PubMed ID: 9689669
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  • 11. 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 Jun; 52(6):471-7. PubMed ID: 17050329
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  • 12. 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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  • 14. 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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  • 17. Heterogeneous spectrum of mutations in CFTR gene from Indian patients with congenital absence of the vas deferens and their association with cystic fibrosis genetic modifiers.
    Sharma H, Mavuduru RS, Singh SK, Prasad R.
    Mol Hum Reprod; 2014 Sep 01; 20(9):827-35. PubMed ID: 24958810
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  • 18. Outcome of intracytoplasmic sperm injection for a couple in which the man is carrier of CFTR p.[R74W;V201M;D1270N] and p.P841R mutations and his spouse a heterozygous carrier of p.F508del mutation of the cystic fibrosis transmembrane conductance regulator gene.
    Brugnon F, Bilan F, Heraud MC, Grizard G, Janny L, Creveaux I.
    Fertil Steril; 2008 Nov 01; 90(5):2004.e23-6. PubMed ID: 18703181
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  • 20. [Agenesis of vas deferens and cystic fibrosis].
    Calleja Escudero J, Telleria Orriols JJ, Estébanez Zarranz J, Alonso Ramos MJ, Amón Sesmero JH, Martínez-Sagarra JM, Blanco Quirós A.
    Actas Urol Esp; 1997 Sep 01; 21(8):773-6. PubMed ID: 9412228
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