H Lomícková, E Seemanová, O Snobl, P Zoban. Show Affiliations »
Abstract
Entities: Disease
Mesh: See more » ChildEye Diseases/geneticsFemaleHumansIntellectual Disability/geneticsMaleOsteoporosis/geneticsSyndrome
Year: 1984 PMID: 6488369
Source DB: PubMed Journal: Cesk Oftalmol ISSN: 0009-059X