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50 积分 2023-03-17 加入
Inheritance of polyalanine expansion mutation of PHOX2B in congenital central hypoventilation syndrome
13小时前
已完结
静脉血栓栓塞症的遗传学研究有助于病因探索
6个月前
已完结
Comprehensive molecular analysis demonstrates type V collagen mutations in over 90% of patients with classic EDS and allows to refine diagnostic criteria†
1年前
已完结
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