Ping Yu

GUCY2D Gene Loss-of-Function Mutations Responsible for Leber Congenital Amaurosis 1

Y. Huo, M. Qi, F. Xue, 2019 .

Preimplantation and prenatal genetic diagnosis for androgen insensitivity syndrome resulting from a novel deletion/insertion mutation

P. Yu, M. Qi, Y. Ye, 2012, Clinical genetics.

Identification of eight novel mutations and transcript analysis of two splicing mutations in Chinese newborns with MCC deficiency

P. Yu, M. Qi, L. Yang, 2015, Clinical genetics.