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Pubmed for Handhelds

PUBMED FOR HANDHELDS

Journal Abstract Search

145 related items for PubMed ID: 12151438

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  • 2. Mutations in the cystic fibrosis gene in men with congenital bilateral absence of the vas deferens.
    De Braekeleer M, Férec C.
    Mol Hum Reprod; 1996 Sep; 2(9):669-77. PubMed ID: 9239681
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  • 3. 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 Sep; 16(2):143-56. PubMed ID: 10923036
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  • 4. Cystic fibrosis and infertility caused by congenital bilateral absence of the vas deferens and related clinical entities.
    Lissens W, Mercier B, Tournaye H, Bonduelle M, Férec C, Seneca S, Devroey P, Silber S, Van Steirteghem A, Liebaers I.
    Hum Reprod; 1996 Dec; 11 Suppl 4():55-78; discussion 79-80. PubMed ID: 9147111
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  • 5. Cystic fibrosis transmembrane conductance regulator (CFTR) gene abnormalities in Indian males with congenital bilateral absence of vas deferens & renal anomalies.
    Gajbhiye R, Kadam K, Khole A, Gaikwad A, Kadam S, Shah R, Kumaraswamy R, Khole V.
    Indian J Med Res; 2016 May; 143(5):616-23. PubMed ID: 27488005
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  • 9. Mutations in the cystic fibrosis transmembrane regulator gene and in vivo transepithelial potentials.
    Wilschanski M, Dupuis A, Ellis L, Jarvi K, Zielenski J, Tullis E, Martin S, Corey M, Tsui LC, Durie P.
    Am J Respir Crit Care Med; 2006 Oct 01; 174(7):787-94. PubMed ID: 16840743
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  • 11. Identification of the second CFTR mutation in patients with congenital bilateral absence of vas deferens undergoing ART protocols.
    Giuliani R, Antonucci I, Torrente I, Grammatico P, Palka G, Stuppia L.
    Asian J Androl; 2010 Nov 01; 12(6):819-26. PubMed ID: 20657600
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  • 15. CFTR p.Arg117His associated with CBAVD and other CFTR-related disorders.
    Thauvin-Robinet C, Munck A, Huet F, de Becdelièvre A, Jimenez C, Lalau G, Gautier E, Rollet J, Flori J, Nové-Josserand R, Soufir JC, Haloun A, Hubert D, Houssin E, Bellis G, Rault G, David A, Janny L, Chiron R, Rives N, Hairion D, Collignon P, Valeri A, Karsenty G, Rossi A, Audrézet MP, Férec C, Leclerc J, Georges Md, Claustres M, Bienvenu T, Gérard B, Boisseau P, Cabet-Bey F, Cheillan D, Feldmann D, Clavel C, Bieth E, Iron A, Simon-Bouy B, Izard V, Steffann J, Viville S, Costa C, Drouineaud V, Fauque P, Binquet C, Bonithon-Kopp C, Morris MA, Faivre L, Goossens M, Roussey M, Girodon E, collaborating working group on p.Arg117His.
    J Med Genet; 2013 Apr 01; 50(4):220-7. PubMed ID: 23378603
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  • 18. Congenital absence of vas deferens and cystic fibrosis.
    Leonardi S, Bombace V, Rotolo N, Sciuto C, La Rosa M.
    Minerva Pediatr; 2003 Feb 01; 55(1):43-7, 47-50. PubMed ID: 12660625
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