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Kaixiang Cheng

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Endocrine|May 7, 2016

Clinical and molecular manifestation of fifteen 17OHD patients: a novel mutation and a founder effectBing Han, Liqiong Xue, Mengxia Fan, et al.

Clinical Endocrinology|March 27, 2014

Phenotypic and molecular characteristics in eleven Chinese patients with 5α-reductase Type 2 deficiencyHui Zhu, Wei Liu, Bing Han, et al.

Human Genetics|March 28, 2018

Next-generation sequencing reveals genetic landscape in 46, XY disorders of sexual development patients with variable phenotypesHao Wang, Lele Zhang, Nan Wang, et al.

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Search research articles

Showing results (21-30 of 23) with videos related to

Sort By:

Pageof 3

You have reached the last page of results.This site can display upto 23 results.

Endocrine|May 7, 2016

Clinical and molecular manifestation of fifteen 17OHD patients: a novel mutation and a founder effectBing Han, Liqiong Xue, Mengxia Fan, et al.

Clinical Endocrinology|March 27, 2014

Phenotypic and molecular characteristics in eleven Chinese patients with 5α-reductase Type 2 deficiencyHui Zhu, Wei Liu, Bing Han, et al.

Human Genetics|March 28, 2018

Next-generation sequencing reveals genetic landscape in 46, XY disorders of sexual development patients with variable phenotypesHao Wang, Lele Zhang, Nan Wang, et al.

Pageof 3