Expanding the phenotypic and genetic spectrum of Chinese patients with congenital absence of vas deferens bearing CFTR and ADGRG2 alleles
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Title
Expanding the phenotypic and genetic spectrum of Chinese patients with congenital absence of vas deferens bearing CFTR
and ADGRG2
alleles
Authors
Keywords
-
Journal
Andrology
Volume -, Issue -, Pages -
Publisher
Wiley
Online
2019-02-28
DOI
10.1111/andr.12592
References
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Related references
Note: Only part of the references are listed.- X-linked ADGRG2 mutation and obstructive azoospermia in a large Pakistani family
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