Lv11
70 积分 2022-09-22 加入
[HEXB gene study and prenatal diagnosis for a family affected by infantile Sandhoff disease]
5个月前
已完结
[Mutational analysis of the methyl-CpG-binding protein 2 (MECP2) gene in male autism patients]
5个月前
已关闭
[Mutation analysis of the SCN1A gene in severe myoclonic epilepsy of infancy]
5个月前
已完结
[Clinical and genetic characteristics of 62 children with mitochondrial epilepsy]
6个月前
已完结
[Clinical phenotypes of TBC1D24 gene related epilepsy]
6个月前
已完结
Genomic landscapes of Chinese sporadic autism spectrum disorders revealed by whole-genome sequencing
6个月前
已完结
Genomic landscapes of Chinese sporadic autism spectrum disorders revealed by whole-genome sequencing
6个月前
已完结
Tumor‐Derived Interleukin 35 Promotes Fibrosis in the Tumor Microenvironment of Pancreatic Cancer by Activating Pancreatic Stellate Cells
7个月前
已完结
Mapping the Non‐Canonical Splicing Variants: Decrypting the Hidden Genetic Architecture of Idiopathic Male Infertility
8个月前
已完结
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