Molecular screening of the CFTR gene in men with anomalies of the vas deferens: identification of three novel mutations
Author:
Publisher
Oxford University Press (OUP)
Subject
Cell Biology,Developmental Biology,Obstetrics and Gynaecology,Genetics,Molecular Biology,Embryology,Reproductive Medicine
Link
http://academic.oup.com/molehr/article-pdf/6/12/1063/9894307/061063.pdf
Cited by 34 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. Compound heterozygous mutations in CFTR causing congenital bilateral absence of the vas deferens in a Chinese pedigree;Molecular Genetics & Genomic Medicine;2024-01
2. Congenital Bilateral Absence of the Vas Deferens;Reference Module in Biomedical Sciences;2024
3. A novel compound heterozygous mutation in CFTR causing congenital bilateral absence of the vas deferens in a Chinese pedigree;2023-05-04
4. Correlation between CFTR variants and outcomes of ART in patients with CAVD in Central China;Scientific Reports;2023-01-05
5. Genetic analysis and intracytoplasmic sperm injection outcomes of Chinese patients with congenital bilateral absence of vas deferens;Journal of Assisted Reproduction and Genetics;2022-02-04
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