J P Fryns, F Dhondt, L Lindemans, H Van den Berghe. Show Affiliations »
Abstract
Entities: Disease
Mesh: See more » Abnormalities, Multiple/diagnosisAtrophyHumansInfant, NewbornMalePigmentation Disorders/congenitalPigmentation Disorders/diagnosisSkin Diseases/congenitalSyndrome
Year: 1978 PMID: 665231
Source DB: PubMed Journal: Acta Paediatr Belg ISSN: 0001-6535