Genetic diagnosis and sperm retrieval outcomes for Chinese patients with congenital bilateral absence of vas deferens-Reference-Cited by-同舟云学术

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Genetic diagnosis and sperm retrieval outcomes for Chinese patients with congenital bilateral absence of vas deferens

Published:2020-02-25 Issue:5 Volume:8 Page:1064-1069
ISSN:2047-2919
Container-title:Andrology
language:en
Short-container-title:Andrologia

Author:

Wang Hongxiang¹,An Miao²,Liu Yidong¹,Hu Kai¹,Jin Yan¹,Xu Shiran¹,Chen Bin¹,Lu Mujun¹^ORCID

Affiliation:

1. Department of Urology and Andrology School of Medicine Renji Hospital Shanghai Jiao Tong University Shanghai China

2. CarrierGene Biotechnologies Co., Ltd Shanghai China

Publisher

Wiley

Subject

Urology,Endocrinology,Reproductive Medicine,Endocrinology, Diabetes and Metabolism

Link

https://onlinelibrary.wiley.com/doi/pdf/10.1111/andr.12769

Reference37 articles.

1. Sexual dysfunction and male infertility

2. Ultrasound of the male genital tract in relation to male reproductive health

3. Congenital bilateral absence of the vas deferens (CBAVD) and cystic fibrosis transmembrane regulator (CFTR): correlation between genotype and phenotype

4. The Genetic Basis of Congenital Bilateral Absence of the Vas Deferens and Cystic Fibrosis

Cited by 10 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. An overview of CFTR mutation profiles and assisted reproductive technology outcomes in Chinese patients with congenital obstructive azoospermia;Journal of Assisted Reproduction and Genetics;2023-12-20

2. Proteomic approach towards identification of seminal fluid biomarkers from individuals with severe oligozoospermia, cryptozoospermia and non-obstructive azoospermia: a pilot study;Translational Andrology and Urology;2023-10

3. Compound heterozygous variants in CFTR with potentially reducing ATP‐binding ability identified in Chinese infertile brothers with isolated congenital bilateral absence of vas deferens;Molecular Genetics & Genomic Medicine;2023-07-24

4. A novel ADGRG2 truncating variant associated with X-linked obstructive azoospermia in a large Chinese pedigree;Journal of Assisted Reproduction and Genetics;2023-06-05

5. Loss-of-function CFTR p.G970D missense mutation might cause congenital bilateral absence of the vas deferens and be associated with impaired spermatogenesis;Asian Journal of Andrology;2023

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