Molecular screening ofCFTRgene in Egyptian patients with congenital bilateral absence of the vas deferens: a preliminary study
Author:
Affiliation:
1. Clinical and Chemical Pathology Department; Faculty of Medicine; Cairo University; Cairo Egypt
2. Andrology and Sexology Department; Faculty of Medicine; Cairo University; Cairo Egypt
Funder
Cairo University
Publisher
Wiley
Subject
Urology,Endocrinology,General Medicine
Link
http://onlinelibrary.wiley.com/wol1/doi/10.1111/and.12563/fullpdf
Reference21 articles.
1. CFTR gene mutations in Japanese individuals with congenital bilateral absence of the vas deferens;Anzai;J Cyst Fibros,2003
2. Mutations in the cystic fibrosis gene in patients with congenital absence of the vas deferens;Chillón;N Engl J Med,1995
3. Spectrum of CFTR mutations in cystic fibrosis and in congenital absence of the vas deferens in France;Claustres;Hum Mutat,2000
4. Analysis of the whole CFTR coding regions and splice junctions in azoospermic men with congenital bilateral aplasia of epididymis or vas deferens;Culard;Hum Genet,1994
5. Best practice guidelines for molecular genetic diagnosis of cystic fibrosis and CFTR-related disorders-updated European recommendations;Dequeker;Eur J Hum Genet,2009
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3. Genetic mutation analysis of 22 patients with congenital absence of vas deferens: a single-center study;Biology of Reproduction;2021-10-21
4. The CFTR gene mild variants poly-T, TG repeats and M470V detection in Indian men with congenital bilateral absence of vas deferens;Andrologia;2017-08-03
5. CFTR Gene Mutations in the Egyptian Population: Current and Future Insights for Genetic Screening Strategy;Frontiers in Genetics;2017-03-31
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