Xiaofei Chen

[A de novo mutation of P gene causes oculocutaneous albinism type 2 with prenatal diagnosis].

Yanfang Zhong, Weiying Jiang, Hongyi Li, 2013, Zhonghua yi xue yi chuan xue za zhi = Zhonghua yixue yichuanxue zazhi = Chinese journal of medical genetics.

Identification of novel variations of oculocutaneous albinism type 2 with Prader–Willi syndrome/Angelman syndrome in two Chinese families

Jie Lei, Z. Fang, Hongyi Li, 2023, Frontiers in Genetics.