R Happle. Show Affiliations »
Abstract
Entities: Disease Species
Mesh: See more » Chromosome MappingChromosomes, Human, Pair 9HumansIncontinentia Pigmenti/geneticsPigmentation Disorders/genetics
Year: 1987 PMID: 3804339 DOI: 10.1007/bf00273854
Source DB: PubMed Journal: Hum Genet ISSN: 0340-6717 Impact factor: 4.132