Lv3
310 积分 2023-02-07 加入
Genetic Evaluation of 114 Chinese Short Stature Children in the Next Generation Era: a Single Center Study
2天前
已完结
线粒体tRNAThr A15951G可能是与Leber遗传性视神经病变相关的基因突变
4天前
已完结
Outcomes of vitreoretinal surgery for familial exudative vitreoretinopathy: a systematic review and meta-analysis of the current literature
13天前
已完结
Novel variant c.428T>C in FZD4 gene in a pedigree affected by familial exudative vitreoretinopathy: clinical, functional, and structural characterization
13天前
已完结
[Analyses of coding sequence point mutation and polymorphism of TGFBI gene in Chinese patients with keratoconus]
24天前
已完结
Genetic and clinical findings in a Chinese cohort with Leber congenital amaurosis and early onset severe retinal dystrophy
26天前
已完结
[Analysis of clinical manifestations and genetic variants among 11 Chinese pedigrees affected with Leber congenital amaurosis]
27天前
已完结
Peripheral Macular Endothelial Dystrophy: Clinical, Histopathologic, Genetic and Functional Characterization
1个月前
已关闭
Association of macular corneal dystrophy with excessive cell senescence and apoptosis induced by the novel mutant CHST6
1个月前
已完结
Mutational spectrum of the SLC4A11 gene in autosomal recessive congenital hereditary endothelial dystrophy
1个月前
已关闭
皖公网安备34019202002308
