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8 积分 2024-12-28 加入
Further Delineation of the Proximal 16p11.2 Microdeletion Syndrome: Novel Findings Among 22 New Individuals
2天前
已完结
9号染色体三体、嵌合体及单亲二体的临床特征及遗传学诊断
4个月前
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[Clinical and genetic analysis of a case of Turner syndrome with rapidly progressive puberty and a literature review]
8个月前
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产前诊断胎儿新发复杂性染色体重排一例
1年前
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平山病合并Chiari畸形1例报道
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