J CAFFEY. Show Affiliations »
Abstract
Entities: Disease Mutation
Keywords: BONE DISEASES/in infant and child
Mesh: See more » Bone DiseasesChildHumansHyperostosis, Cortical, CongenitalInfant
Year: 1957 PMID: 13431894 PMCID: PMC1889299
Source DB: PubMed Journal: Proc R Soc Med ISSN: 0035-9157