Associated Papers
Congenital Bilateral Absence of the Vas Deferens.
Cai Z et al.
Frontiers in Genetics, 2022
Expanding the phenotypic and genetic spectrum of Chinese patients with congenital absence of vas deferens bearing CFTR and ADGRG2 alleles.
Yuan P et al.
Andrology, 2019
Genetic defects in human azoospermia.
Ghieh F et al.
Basic and Clinical Andrology, 2019
X-linked ADGRG2 mutation and obstructive azoospermia in a large Pakistani family.
Khan MJ et al.
Scientific Reports, 2018
A systematic review on the genetics of male infertility in the era of next-generation sequencing.
Robay A et al.
Arab Journal of Urology, 2018
Pathogenic role of ADGRG2 in CBAVD patients replicated in Chinese population.
Yang B et al.
Andrology, 2017
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