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注意:仅列出部分参考文献,下载原文获取全部文献信息。Loss-of-Function Mutations in SOX10 Cause Kallmann Syndrome with Deafness
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Mutations in CHD7, Encoding a Chromatin-Remodeling Protein, Cause Idiopathic Hypogonadotropic Hypogonadism and Kallmann Syndrome
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