Liping Wang
2PUBLICATIONS
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Publications (2)
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|Jun 01, 2021
A de novo 10q11.23q22.1 deletion detected by whole genome mate-pair sequencing: a case report.Dalin Fu, Weisheng Lin, Fen Lu
|Feb 17, 2021
A case report of congenital idiopathic hypogonadotropic hypogonadism caused by novel mutation of GNRHR gene.Liping Wang, Weisheng Lin, Xiaohong Li
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