A E Lin. Show Affiliations »
Abstract
Entities: Disease
Mesh: See more » HumansNoonan Syndrome/genetics
Year: 1988 PMID: 3351898 PMCID: PMC1015430 DOI: 10.1136/jmg.25.1.64-a
Source DB: PubMed Journal: J Med Genet ISSN: 0022-2593 Impact factor: 6.318