CFTR Haplotype Analysis Reveals Genetic Heterogeneity in the Etiology of Congenital Bilateral Aplasia of the Vas Deferens

Congenital bilateral aplasia of the vas deferens (CBAVD) was suggested to be a mild form of cystic fibrosis (CF). Mutation analysis of the cystic fibrosis transmembrane conductance regulator (CFTR) gene in males with CBAVD revealed that in some males CBAVD is caused by two defective CFTR alleles. Th...

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Detaylı Bibliyografya
Asıl Yazarlar: Rave-Harel, Naama, Madgar, Igael, Goshen, Ran, Nissim-Rafinia, Malka, Ziadni, Anuar, Rahat, Ayelet, Chiba, Ornit, Kalman, Yoram M, Brautbar, Chaim, Levinson, David, Augarten, Arie, Kerem, Eitan, Kerem, Batsheva
Materyal Türü: Artigo
Dil:Inglês
Baskı/Yayın Bilgisi: 1995
Konular:
Original Articles
Online Erişim:https://ncbi.nlm.nih.gov/pmc/articles/PMC1801105/
https://ncbi.nlm.nih.gov/pubmed/7539210
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