Extensive analysis of 40 infertile patients with congenital absence of the vas deferens: in 50% of cases only one CFTR allele could be detected-Reference-Cited by-同舟云学术

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Extensive analysis of 40 infertile patients with congenital absence of the vas deferens: in 50% of cases only one CFTR allele could be detected

Published:1995-02 Issue:2 Volume:95 Page:
ISSN:0340-6717
Container-title:Human Genetics
language:en
Short-container-title:Hum Genet

Author:

Casals T.,Bassas L.,Ruiz-Romero J.,Chill�n M.,Gim�nez J.,Ramos M.D.,Tapia G.,Narv�ez H.,Nunes V.,Estivill X.

Publisher

Springer Science and Business Media LLC

Subject

Genetics (clinical),Genetics

Link

http://link.springer.com/content/pdf/10.1007/BF00209403.pdf

Cited by 62 articles. 订阅此论文施引文献订阅此论文施引文献，注册后可以免费订阅5篇论文的施引文献，订阅后可以查看论文全部施引文献

1. TG12-T5-V470 haplotype in the CFTR gene is associated with non-obstructive azoospermia in Iranian infertile men;Gene Reports;2021-06

2. Cutting-Edge Evaluation of Male Infertility;Urologic Clinics of North America;2020-05

3. Cystic Fibrosis;Emery and Rimoin's Principles and Practice of Medical Genetics and Genomics;2020

4. Diagnostics of CFTR-negative patients with congenital bilateral absence of vas deferens: which mutations are of most interest?;Expert Review of Molecular Diagnostics;2019-12-23

5. VX-770-mediated potentiation of numerous human CFTR disease mutants is influenced by phosphorylation level;Scientific Reports;2019-09-17

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