I Helin, U Jodal. Show Affiliations »
Abstract
Entities: Disease
Mesh: See more » Abnormalities, Multiple/geneticsFemaleHumansHypoproteinemia/complicationsHypoproteinemia/geneticsInfantInfant, NewbornMaleNose/abnormalitiesSitus Inversus/complicationsSitus Inversus/geneticsSyndrome
Year: 1981 PMID: 7310588 DOI: 10.1016/s0022-3476(81)80026-1
Source DB: PubMed Journal: J Pediatr ISSN: 0022-3476 Impact factor: 4.406