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[Mutation analysis and prenatal diagnosis of FBN1 gene mutations for four patients with Marfan syndrome]
14小时前
待确认
马凡综合征一家系的FBN1致病基因突变分析及产前诊断
14小时前
待确认
Tuberous Sclerosis Complex
2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
2个月前
已完结
[Genetic analysis of a child with 13q deletion syndrome featuring congenital heart disease]
4个月前
已完结
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