Lv1
70 积分 2024-03-29 加入
Deleterious, protein-altering variants in GSPT2 are putatively associated with an X-linked neurodevelopmental disorder with intellectual disability, language impairment, autism and epilepsy
4个月前
已关闭
Rare loss-of-function variants reveal threshold and multifactorial inheritance of dextrocardia
4个月前
已完结
Noninvasive prediction models of intra-amniotic infection in women with preterm labor
6个月前
已完结
Non-invasive prenatal testing for aneuploidy screening
6个月前
已完结
Genome Wide and Rare Variant Association Studies of Amblyopia in the All of Us Research Program
8个月前
已完结
Genome Wide and Rare Variant Association Studies of Amblyopia in the All of Us Research Program
8个月前
已完结
Exome sequencing identifies NMNAT1 mutations as a cause of Leber congenital amaurosis
8个月前
已完结
Exploring gene expression signatures in preeclampsia and identifying hub genes through bioinformatic analysis
9个月前
已关闭
MiR-22-3p Suppresses Vascular Remodeling and Oxidative Stress by Targeting CHD9 during the Development of Hypertension
10个月前
已完结
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