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[Clinical characteristics and genetic features of benign infantile epilepsy with PRRT2 mutation]
3个月前
已完结
Endodontic management of a hypertaurodontic tooth associated with 48, XXYY syndrome: A review and case report
3个月前
已完结
Disseminated BCG Disease in a Patient with Hyper IgE Syndrome due to Dominant-Negative STAT3 Mutation—Case Report
3个月前
已完结
A challenging differential diagnosis in a patient with autosomal dominant STAT3 deficiency
3个月前
已完结
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