Xu F, Zhang YN, Cheng DH, Tan K, Zhong CG, Lu GX, Lin G, Tan YQ*. The first patient with a pure 1p36 microtriplication associated with severe clinical phenotypes

Pre One:He WB, Banerjee S, Meng LL, Du J, Gong F, Huang H, Zhang XX, Wang YY, Lu GX, Lin G, Tan YQ*. Whole-exome sequencing identifies a homozygous donor splice-site mutation in STAG3 that causes primary ovarian insufficiency

Next One:Yuan SM, Meng LL, Zhang Y, Tu CF, Du J, Li W, Liang P, Lu GX, Tan YQ*. Genotype-phenotype correlation and identification of two novel SRD5A2 mutations in 33 Chinese patients with hypospadias