ArticleMedicine2020
A novel FGFR2 (S137W) mutation resulting in Apert syndrome: A case report.
Qingyang Shi et al.PubMed ↗Full text ↗Publisher ↗
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ArticleMedicine2020
Qingyang Shi et al.PubMed ↗Full text ↗Publisher ↗
No numbers read from the abstract.