Wan-ling Wu

Identifying a novel mutation of CYP17A1 gene from five Chinese 17α-hydroxylase/17, 20-lyase deficiency patients.

Chao Xu, Bing-Li Liu, Wei Liu, 2013, Gene.

A unique exonic splicing mutation in the CYP17A1 gene as the cause for steroid 17{alpha}-hydroxylase deficiency.

Bing-Li Liu, Wei Liu, C. Pan, 2011, European journal of endocrinology.

A splice site mutation combined with a novel missense mutation of LHCGR cause male pseudohermaphroditism

Bing-Li Liu, Huai-Dong Song, Ying Ru, 2009, Human mutation.

Zinc transporter ZIP12 maintains zinc homeostasis and protects spermatogonia from oxidative stress during spermatogenesis

Chenyi Jiang, Li Wang, Chengxuan Yu, 2021, Reproductive Biology and Endocrinology.

Identification of steroid biosynthetic defects in genotype‐proven heterozygous individuals for 17α‐hydroxylase/17,20‐lyase deficiency

Bing-Li Liu, Huai-Dong Song, Yan Gu, 2010, Clinical endocrinology.

Identification of a novel mutation in CYP17A1 gene.

Bing-Li Liu, Wei Liu, C. Pan, 2013, Translational research : the journal of laboratory and clinical medicine.

Genetic diagnosis and weight loss surgery of a case of Prader-Willi syndrome

Jian-jun Yang, Bing-Li Liu, Huai-Dong Song, 2011 .