M Frontali, M Ramenghi, S Trabace, B Dallapiccola. Show Affiliations »
Abstract
Entities: Disease
Mesh: See more » Abnormalities, Multiple/geneticsChromosome DeletionChromosomes, Human, 6-12 and X/ultrastructureHumansSyndrome
Year: 1982 PMID: 7143397 PMCID: PMC1048932 DOI: 10.1136/jmg.19.5.390-a
Source DB: PubMed Journal: J Med Genet ISSN: 0022-2593 Impact factor: 6.318