Tan YQ, Yin XY, Zhang SP, Jiang H, Tan K, Li J, Xiong B, Gong F, Zhang CL, Pan XY, Chen F, Chen SP, Gong C, Lu CF, Luo KL, Gu YF, Zhang XQ, Wang W, Xu X, Vajta G, Bolund L, Yang HM, Lu GX, Du YT, Lin G. Clinical outcome of preimplantation genetic diagnosis and screening using next generation sequencing

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