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A Novel Hemizygous Frameshift OPHN1 Gene Mutation Associated with Mental Retardation, X-Linked, with Cerebellar Hypoplasia and Distinctive Facial Appearance
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Scientific Publications
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A Novel Hemizygous Frameshift OPHN1 Gene Mutation Associated with Mental Retardation, X-Linked, with Cerebellar Hypoplasia and Distinctive Facial Appearance
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