J H Korn. Show Affiliations »
Abstract
Entities: Disease
Mesh: See more » HumansRaynaud Disease/geneticsRaynaud Disease/pathologyScleroderma, Systemic/geneticsScleroderma, Systemic/pathologySyndrome
Year: 2000 PMID: 11092200 DOI: 10.1097/00002281-200011000-00006
Source DB: PubMed Journal: Curr Opin Rheumatol ISSN: 1040-8711 Impact factor: 5.006