S Yetgin, C Altay, Y Laleli. Show Affiliations »
Abstract
Entities: Disease
Mesh: See more » Anemia, Megaloblastic/geneticsChildChild, PreschoolConsanguinityFemaleHumansInfantMalabsorption Syndromes/geneticsMaleProteinuria/geneticsVitamin B 12 Deficiency/genetics
Year: 1978 PMID: 757016
Source DB: PubMed Journal: Turk J Pediatr ISSN: 0041-4301 Impact factor: 0.552