Additional file 1 of The first familial NSD2 cases with a novel variant in a Chinese father and daughter with atypical WHS facial features and a 7.5-year follow-up of growth hormone therapy
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Additional file 1: Table S1. Clinical manifestation comparison in WHS patients and NSD2 truncating mutation cases.
补充材料1：表S1 沃-霍综合征（WHS）患者与NSD2截短突变病例的临床表型对比
创建时间：
2020-12-04
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