Refreshing results…
Clinical presentation of calmodulin mutations: the International Calmodulinopathy Registry
UploadKBG syndrome: Common and uncommon clinical features based on 31 new patients
Download from api.wiley.comA heterozygous, intragenic deletion of CNOT2 recapitulates the phenotype of 12q15 deletion syndrome
Download from api.wiley.comMissing publications? Search for publications with a matching author name.