H Brehme, F Härle. Show Affiliations »
Abstract
Entities: Disease Species
Mesh: See more » DermatoglyphicsFemaleFootGenetics, MedicalHandHumansMalePierre Robin Syndrome/diagnosis
Year: 1971 PMID: 5114671 DOI: 10.1007/bf00295799
Source DB: PubMed Journal: Humangenetik ISSN: 0018-7348