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An Exploration of Mutagenesis in a Family with Cleidocranial Dysplasia without RUNX2 Mutation https://t.co/B7E45OCinQ
An Exploration of Mutagenesis in a Family with Cleidocranial Dysplasia without RUNX2 Mutation https://t.co/B7E45OCinQ
New Research: An Exploration of Mutagenesis in a Family with Cleidocranial Dysplasia without RUNX2 Mutation: Cleidocranial dysplasia (CCD) is an autosomal dominant inheritable skeletal disorder characterized by cranial dysplasia, clavicle… https://t.co/Kz2