Peikuan Cong

发表

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.

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.

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.

Genomic organization and promoter analysis of the Trichomonas vaginalis core histone gene families.

Songnian Hu, Weidong Bao, Yingfeng Luo, 2010, Parasitology international.

Exome sequencing identifies NMNAT1 mutations as a cause of Leber congenital amaurosis

Renhua Wu, Yanhua Chen, Xin Yi, 2012, Nature Genetics.

LOVD–DASH: A comprehensive LOVD database coupled with diagnosis and an at‐risk assessment system for hemoglobinopathies

M. Qi, Shanhuo Yan, Yuehong Zhou, 2019, Human mutation.

Novel LOVD databases for hereditary breast cancer and colorectal cancer genes in the Chinese population

Tao Zhang, Ying Yuan, Peter Hu, 2011, Human mutation.

Familial syndrome resembling Aarskog syndrome

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

Colby T. Ford, Lipika R. Pal, Meng Wang, 2019 .