Wei-lin Tang

Novel inactivating mutations in the FSH receptor cause premature ovarian insufficiency with resistant ovary syndrome.

Juan Du, G. Lin, Yueqiu Tan, 2019, Reproductive biomedicine online.

A novel AVPR2 missense mutation in a Chinese boy with severe inherited nephrogenic diabetes insipidus

Wen Li, G. Lu, G. Lu, 2011, Journal of pediatric endocrinology & metabolism : JPEM.

A Chinese family with Oguchi’s disease due to compound heterozygosity including a novel deletion in the arrestin gene

Wen Li, G. Lu, Wei-lin Tang, 2012, Molecular vision.

Clinical and genetic analysis of classical Ehlers‐Danlos syndrome patient caused by synonymous mutation in COL5A2

Jing Liu, Ying Peng, Zhenhua Zhu, 2021, Molecular genetics & genomic medicine.