R M Hays, L E Bartoshesky, M Feingold. Show Affiliations »
Abstract
Entities: Disease
Mesh: See more » Abnormalities, Multiple/geneticsEdema/geneticsFemaleFollow-Up StudiesGastrointestinal Diseases/geneticsGenes, RecessiveHumansHyperhidrosis/geneticsInfantInfant, NewbornMaleRadius/abnormalitiesSyndromeThrombocytopenia/genetics
Year: 1982 PMID: 7139091
Source DB: PubMed Journal: Birth Defects Orig Artic Ser ISSN: 0547-6844