Lv12
60 积分 2025-02-27 加入
Spatiotemporal transcriptome atlas of human embryos after gastrulation
4小时前
已完结
Prevalence of BRCA1/BRCA2 pathogenic variation in Chinese Han population
1个月前
已完结
Chromatin state dynamics confers specific therapeutic strategies in enhancer subtypes of colorectal cancer
1个月前
已完结
Structural basis for LZTR1 recognition of RAS GTPases for degradation
1个月前
已完结
Exome Sequencing to Identify Novel Susceptibility Genes for Nonsyndromic Split‐Hand/Ft Malformation: A Report From the National Birth Defects Prevention Study
1个月前
已完结
Pathogenic Mechanisms in Congenital Afibrinogenemia: A Systematic Review of Genetic Variants
2个月前
已完结
eP326: Genome sequencing reveals BHLHA9 gene duplication as cause of multi-generational split-hand/foot malformation with long bone deficiency
5个月前
已完结
Comprehensive analysis of Chinese patients with non-LPL familial chylomicronemia syndrome: Genetic variants, dietary interventions, and clinical insights
6个月前
已完结
Non-invasive prenatal testing for dominant single-gene disorders using targeted next-generation sequencing
6个月前
已完结
Genetics of glycosylation in mammalian development and disease
7个月前
已完结
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