B C Mehta, M B Agarwal. Show Affiliations »
Abstract
Entities: Disease
Mesh: See more » AdolescentAdultAfibrinogenemia/diagnosisBlood Coagulation Disorders/diagnosisBlood Coagulation Disorders/geneticsChildChild, PreschoolFactor XI Deficiency/geneticsFactor XIII Deficiency/geneticsFemaleHemophilia A/diagnosisHemophilia B/diagnosisHumansInfantInfant, NewbornMalevon Willebrand Diseases/genetics
Year: 1981 PMID: 6976934 DOI: 10.1007/BF02822303
Source DB: PubMed Journal: Indian J Pediatr ISSN: 0019-5456 Impact factor: 1.967