A N Campbell, J Inglis, A S Paynter. Show Affiliations »
Abstract
Entities: Disease
Mesh: See more » Anemia, Macrocytic/geneticsAnemia, Megaloblastic/geneticsFemaleGrowth Disorders/geneticsHumansInfantMaleProteinuria/geneticsSyndromeVitamin B 12 Deficiency/genetics
Year: 1981 PMID: 7301700 PMCID: PMC2426111 DOI: 10.1136/pgmj.57.670.509
Source DB: PubMed Journal: Postgrad Med J ISSN: 0032-5473 Impact factor: 2.401