C Schepis, P Failla, M Siragusa, C Romano. Show Affiliations »
Abstract
Mesh: See more » ChildChromosomes, Human, Pair 13/geneticsFemaleHumansMosaicismPigmentation Disorders/geneticsPigmentation Disorders/pathologySkin/pathologyTrisomy
Year: 2001 PMID: 11244237 DOI: 10.1159/000051593
Source DB: PubMed Journal: Dermatology ISSN: 1018-8665 Impact factor: 5.366