Qiaolian Wen

Mutation analysis of Connexon43 gene in Chinese patients with congenital heart defects.

Mugen Liu, Shiguo Liu, Binbin Wang, 2010, International journal of cardiology.

Variations of CITED2 Are Associated with Congenital Heart Disease (CHD) in Chinese Population

Xu Ma, Congmin Li, Yuan Wu, 2014, PloS one.

Mutational analysis of human bone morphogenetic protein 15 in Chinese women with polycystic ovary syndrome.

Jingjing Liu, Binbin Wang, Jing Wang, 2011, Metabolism: clinical and experimental.

Mutations in the cystic fibrosis transmembrane conductance regulator (CFTR) in Chinese patients with congenital bilateral absence of vas deferens.

Xinyu Zhang, Binbin Wang, Longfei Cheng, 2012, Journal of cystic fibrosis : official journal of the European Cystic Fibrosis Society.

Interleukin 1 beta (IL-1β) promoter C [−511] T polymorphism but not C [+3953] T polymorphism is associated with polycystic ovary syndrome

Jingjing Liu, Binbin Wang, Jing Wang, 2010, Endocrine.

Identification of a Novel Mutation in a Pseudohypoparathyroidism Family

Binbin Wang, Xu Ma, Zhi-min Miao, 2011, International journal of endocrinology.

Analyses of growth differentiation factor 9 (GDF9) and bone morphogenetic protein 15 (BMP15) mutation in Chinese women with premature ovarian failure

Binbin Wang, Jing Wang, Xu Ma, 2010, Clinical endocrinology.

Mutation analysis of FOXL2 gene in Chinese patients with premature ovarian failure

Binbin Wang, Jing Wang, Xu Ma, 2010, Gynecological endocrinology : the official journal of the International Society of Gynecological Endocrinology.

Analyses of growth differentiation factor 9 (GDF9) and bone morphogenetic protein 15 (BMP15) mutation in Chinese women with premature ovarian failure

Binbin Wang, Jing Wang, Xu Ma, 2010, Clinical endocrinology.