Associated Papers
Congenital Bilateral Absence of the Vas Deferens.
Cai Z et al.
Frontiers in Genetics, 2022
Novel ADGRG2 truncating variants in patients with X-linked congenital absence of vas deferens.
Pagin A et al.
Andrology, 2020
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
Pathogenic role of ADGRG2 in CBAVD patients replicated in Chinese population.
Yang B et al.
Andrology, 2017
Truncating Mutations in the Adhesion G Protein-Coupled Receptor G2 Gene ADGRG2 Cause an X-Linked Congenital Bilateral Absence of Vas Deferens.
Patat O et al.
American Journal of Human Genetics, 2016
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