Gang Wang

A novel AXIN2 mutation and perinatal risk factors contribute to sagittal craniosynostosis: evidence from a monochorionic diamniotic twin family

A. Gu, Qing Yan, Zhenkun Weng, 2020 .

Promoter variant in the catalase gene is associated with vitiligo in Chinese people.

T. Gao, Chunying Li, Kai Li, 2010, The Journal of investigative dermatology.

Polymorphism of MTHFR 1298A>C in relation to adverse pregnancy outcomes in Chinese populations†

Li Tang, Huawei Wang, M. Rao, 2019, Molecular genetics & genomic medicine.

Association of genetic polymorphisms in the type II deiodinase gene with bipolar disorder in a subset of Chinese population

Yongyong Shi, Lin He, Bing He, 2009, Progress in Neuro-Psychopharmacology and Biological Psychiatry.

A novel LMNA indel mutation identified in a family with atrioventricular block and atrial fibrillation

Yimei Du, Zhangrong Jia, Jiyao Xu, 2021, Medicine.

An Axin2 mutation and perinatal risk factors contribute to sagittal craniosynostosis: evidence from a Chinese female monochorionic diamniotic twin family

A. Gu, Qing Yan, Zhenkun Weng, 2021, Hereditas.