Lv1
90 积分 2023-09-02 加入
Developmental delay and failure to thrive associated with a loss‐of‐function variant in WHSC1 (NSD2)
5小时前
待确认
De novo loss-of-function variants in NSD2 (WHSC1) associate with a subset of Wolf–Hirschhorn syndrome
5小时前
待确认
Expression Analyses of Cep152, a Responsible Gene Product for Autosomal Recessive Primary Microcephaly, during Mouse Brain Development
2个月前
已完结
原发性小头畸形综合征中的 DNA 复制蛋白
6个月前
已完结
时间至关重要：原发性小头畸形的分子机制
6个月前
已完结
Expression Analyses of Cep152, a Responsible Gene Product for Autosomal Recessive Primary Microcephaly, during Mouse Brain Development
6个月前
已关闭
Age-dependent effects of social isolation on mesolimbic dopamine release. Experimental Brain Research
7个月前
已完结
Role of cilia in structural birth defects: Insights from ciliopathy mutant mouse models
11个月前
已完结
Altered GLI3 and FGF8 signaling underlies acrocallosal syndrome phenotypes inKif7depleted mice
11个月前
已完结
A single mutation in the prM protein of Zika virus contributes to fetal microcephaly
1年前
已完结
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