J Goodship. Show Affiliations »
Abstract
Entities: Disease Gene
Mesh: See more » Abnormalities, Multiple/geneticsChromosomes, Human, Pair 22FemaleHumansMaleSyndrome
Year: 1998 PMID: 9863611 PMCID: PMC1051526 DOI: 10.1136/jmg.35.12.1054-a
Source DB: PubMed Journal: J Med Genet ISSN: 0022-2593 Impact factor: 6.318