Jing Yong

A large deletion/insertion-induced frameshift mutation of the androgen receptor gene in a family with a familial complete androgen insensitivity syndrome.

P. Yu, M. Qi, Y. Ye, 2012, Gene.

Familial syndrome resembling Aarskog syndrome

M. Qi, Yan Jiang, Yunsong Yu, 2010, American journal of medical genetics. Part A.

Preimplantational Genetic Diagnosis and Mutation Detection in a Family with Duplication Mutation of DMD Gene

P. Yu, M. Qi, Y. Ye, 2014, Gynecologic and Obstetric Investigation.

A Chinese patient with KBG syndrome and a 9q31.2-33.1 microdeletion.

M. Qi, Yunsong Yu, Mingzhi Xu, 2013, European journal of medical genetics.

Development of a comprehensive real-time PCR assay for dystrophin gene analysis and prenatal diagnosis of Chinese families.

M. Qi, Jiansheng Xie, Yuchan Mao, 2013, Clinica chimica acta; international journal of clinical chemistry.

Familial syndrome resembling Aarskog syndrome

M. Qi, Yunsong Yu, Mingzhi Xu, 2010, American journal of medical genetics. Part A.