M M Cohen, P W Hayden. Show Affiliations »
Abstract
Entities: Disease
Mesh: See more » ChildDiagnosis, DifferentialEye Neoplasms/geneticsFemaleFoot Diseases/geneticsHamartoma/diagnosisHamartoma/geneticsHumansMaleNeurofibromatosis 1/diagnosisNeurofibromatosis 1/geneticsNevus/geneticsScleraSkin Neoplasms/geneticsSyndrome
Year: 1979 PMID: 118782
Source DB: PubMed Journal: Birth Defects Orig Artic Ser ISSN: 0547-6844