Lv3
250 积分 2026-04-20 加入
Molecular mechanisms of mitochondrial dynamics
17小时前
已完结
De novo MEIS2 mutation causes syndromic developmental delay with persistent gastro-esophageal reflux
15天前
已完结
A novel MEIS2 mutation explains the complex phenotype in a boy with a typical NF1 microdeletion syndrome
15天前
已完结
Current status and challenges in prenatal and neonatal screening, diagnosis, and management of congenital heart disease in China
16天前
已完结
22q11.2 microduplication in a family with recurrent fetal congenital heart disease
1个月前
已完结
GRIN2B encephalopathy: novel findings on phenotype, variant clustering, functional consequences and treatment aspects
1个月前
已关闭
The uncertainty of copy number variants: pregnancy decisions and clinical follow-up
4个月前
已完结
Loss of FUT8 impairs embryonic development by reducing cAMP production in granulosa cells FUT8
6个月前
已完结
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