CFTR Mutation Analysis of a Caucasian Father with Congenital Bilateral Absence of Vas Deferens, a Taiwanese Mother, and Twins Resulting from ICSI Procedure

CFTR Mutation Analysis of a Caucasian Father with Congenital Bilateral Absence of Vas Deferens, a Taiwanese Mother, and Twins Resulting from ICSI Procedure

Cystic fibrosis (CF), caused by mutations in the cystic fibrosis transmembrane conductance regulator (CFTR) gene, is one of the most common autosomal recessive diseases in Caucasians. We screened for the CFTR gene mutation in a Caucasian father with congenital bilateral absence of the vas deferens (...

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Bibliographic Details
Main Authors: Han-Sun Chiang, Chien-Chih Wu, Yi-No Wu, Jyh-Feng Lu, Gin-Hong Lin, Jiann-Loung Hwang
Format: Article
Language:English
Published: Elsevier 2008-09-01
Series:Journal of the Formosan Medical Association
Subjects:
CFTR mutation
congenital bilateral absence of the vas deferens
cystic fibrosis
intracytoplasmic single sperm injection
vas deferens
Online Access:http://www.sciencedirect.com/science/article/pii/S0929664608601199

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http://www.sciencedirect.com/science/article/pii/S0929664608601199

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