Meng LL, Yuan SM, Tu CF, Lin G, Lu GX, Tan YQ*. Next-generation sequencing identified a novel SPTB frameshift insertion causing hereditary spherocytosis in China

Pre One:Zhang YX, Li HY, He WB, Tu C, Du J, Li W, Lu GX, Lin G, Yang Y, Tan YQ*. XRCC2 mutation causes premature ovarian insufficiency as well as non-obstructive azoospermia in humans

Next One:Meng L, Tu C, Lu G, Lin G, Tan Y*. Novel biallelic PCNT deletion causing microcephalic osteodysplastic primordial dwarfism type II with congenital heart defect