Результаты поиска - Wen XL

Case Report: A Novel Homozygous Mutation of Cyclin O Gene Mutation in Primary Ciliary Dyskinesia with Short Stature по Gong D, Tang Q, Yan LJ, Ye XM, Yang YC, Zou L, Ji Q, Wen XL

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A Case of Floating-Harbor Syndrome with “Growth and Language Development Delay” as Its Clinical Manifestation по Yang YC, Tang Q, Yan LJ, Zhang SB, Ye XM, Gong D, Zou L, Wen XL

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A Case Report of Cardiofaciocutaneous Syndrome with MAP2K1 Pathogenic Variant по Tang Q, Gong D, Ye XM, Xu JR, Yang YC, Yan LJ, Zou L, Wen XL

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