R Happle, A Kupferschmid. Show Affiliations »
Abstract
Entities: Disease
Mesh: See more » AdultCarcinoma, Basal Cell/geneticsCells, CulturedCervical Vertebrae/abnormalitiesChromosome AberrationsChromosome DisordersCysts/geneticsFacial Neoplasms/geneticsHumansLymphocytesMaleMandibular Diseases/geneticsNevus/geneticsSyndrome
Year: 1972 PMID: 5082099 DOI: 10.1007/bf00702372
Source DB: PubMed Journal: Humangenetik ISSN: 0018-7348