S Sachdeva, G F Smith. Show Affiliations »
Abstract
Entities: Disease
Mesh: See more » Basal Ganglia DiseasesChromosome AberrationsDe Lange Syndrome/geneticsExtrapyramidal TractsHumansMovement Disorders/geneticsMuscular Diseases/congenitalSyndrome
Year: 1973 PMID: 4121247 DOI: 10.1016/s0140-6736(73)90629-6
Source DB: PubMed Journal: Lancet ISSN: 0140-6736 Impact factor: 79.321