T E Kelly, R J Cooke, R W Kester. Show Affiliations »
Abstract
Entities: Disease
Mesh: See more » AdolescentAlbinism/geneticsBone Marrow CellsChildChromosome AberrationsChromosome DisordersCraniofacial Dysostosis/geneticsGrowth Disorders/geneticsHemorrhagic Disorders/geneticsHumansInfant, NewbornIntellectual Disability/geneticsMacrophagesMalePhenotypeSyndrome
Year: 1977 PMID: 890099
Source DB: PubMed Journal: Birth Defects Orig Artic Ser ISSN: 0547-6844