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
发布时间:2020-01-14
点击次数:
影响因子:3.083
发表刊物:Ann Hematol
合写作者:Tan YQ*, Lu GX, Lin G, Tu CF, Yuan SM, Meng LL
文献类型:J
卷号:98
期号:1
页面范围:223-226
是否译文:否
发表时间:2019-01-08
收录刊物:SCI
上一条: 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
下一条: 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