首页>American journal of medical genetics, Part A>A Relatively Mild Skeletal Ciliopathy Phenotype Consistent with Cranioectodermal Dysplasia Is Associated with a Homozygous Nonsynonymous Mutation in WDR35
A Relatively Mild Skeletal Ciliopathy Phenotype Consistent with Cranioectodermal Dysplasia Is Associated with a Homozygous Nonsynonymous Mutation in WDR35
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