J Kirk. Show Affiliations »
Abstract
Entities: Disease Gene
Mesh: See more » Abnormalities, Multiple/geneticsChildChromosomes, Human, Pair 22HumansSyndrome
Year: 1998 PMID: 9863612 PMCID: PMC1051527 DOI: 10.1136/jmg.35.12.1054-b
Source DB: PubMed Journal: J Med Genet ISSN: 0022-2593 Impact factor: 6.318