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Pubmed for Handhelds

PUBMED FOR HANDHELDS

Journal Abstract Search

145 related items for PubMed ID: 12151438

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  • 22. CFTR haplotype analysis reveals genetic heterogeneity in the etiology of congenital bilateral aplasia of the vas deferens.
    Rave-Harel N, Madgar I, Goshen R, Nissim-Rafinia M, Ziadni A, Rahat A, Chiba O, Kalman YM, Brautbar C, Levinson D.
    Am J Hum Genet; 1995 Jun; 56(6):1359-66. PubMed ID: 7539210
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  • 23. The cystic fibrosis transmembrane regulator gene and male infertility.
    Quinzii C, Castellani C.
    J Endocrinol Invest; 2000 Nov; 23(10):684-9. PubMed ID: 11097434
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  • 26. 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; 19(5):1094-100. PubMed ID: 15070876
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  • 29. Airway inflammation and infection in congenital bilateral absence of the vas deferens.
    Gilljam M, Moltyaner Y, Downey GP, Devlin R, Durie P, Cantin AM, Zielenski J, Tullis DE.
    Am J Respir Crit Care Med; 2004 Jan 15; 169(2):174-9. PubMed ID: 14551163
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  • 30. Cystic fibrosis transmembrane conductance regulator gene screening and clinical correlation in Taiwanese males with congenital bilateral absence of the vas deferens.
    Wu CC, Hsieh-Li HM, Lin YM, Chiang HS.
    Hum Reprod; 2004 Feb 15; 19(2):250-3. PubMed ID: 14747162
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  • 31. 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 15; 20(9):827-35. PubMed ID: 24958810
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  • 32. Cystic fibrosis phenotype evaluation and paternity outcome in 50 males with congenital bilateral absence of vas deferens.
    Josserand RN, Bey-Omar F, Rollet J, Lejeune H, Boggio D, Durand DV, Durieu I.
    Hum Reprod; 2001 Oct 15; 16(10):2093-7. PubMed ID: 11574497
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