M Masuno, T Orii. Show Affiliations »
Abstract
Entities: Disease
Mesh: See more » Abnormalities, Multiple/geneticsBrain/abnormalitiesChromosome DeletionChromosomes, Human, Pair 7Eye Abnormalities/geneticsFacial Bones/abnormalitiesHumansSyndrome
Year: 1990 PMID: 2323097 DOI: 10.1111/j.1399-0004.1990.tb03511.x
Source DB: PubMed Journal: Clin Genet ISSN: 0009-9163 Impact factor: 4.438