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

Pre One: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

Next One:Liu Q, Tan YQ*. Advances in Identifications of Susceptibility Gene Defects of Hereditary Colorectal Cancer