S M Pueschel, G Barsel-Bowers. Show Affiliations »
Abstract
Entities: Disease
Mesh: See more » Abnormalities, Multiple/geneticsAdultChromosome Aberrations/diagnosisChromosome DisordersEyelid Diseases/geneticsFace/abnormalitiesFemaleGenes, DominantHumansInfant, NewbornMalePhenotypeSyndrome
Year: 1979 PMID: 501480 DOI: 10.1016/s0022-3476(79)80300-5
Source DB: PubMed Journal: J Pediatr ISSN: 0022-3476 Impact factor: 4.406