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10 积分 2024-12-28 加入
平山病合并Chiari畸形1例报道
3天前
已完结
[Mutation analysis and prenatal diagnosis of FBN1 gene mutations for four patients with Marfan syndrome]
1个月前
已完结
马凡综合征一家系的FBN1致病基因突变分析及产前诊断
1个月前
已完结
Tuberous Sclerosis Complex
3个月前
已完结
Mild TSC phenotype and non-penetrance associated with a frameshift variant in TSC2 prompts caution in evaluating pathogenicity of frameshift variants
3个月前
已完结
[Genetic analysis of a child with 13q deletion syndrome featuring congenital heart disease]
6个月前
已完结
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