Paul Saenger. Show Affiliations »
Abstract
Mesh: See more » HumansMutation, MissenseNoonan Syndrome/diagnosisNoonan Syndrome/genetics
Year: 2002 PMID: 12161468 DOI: 10.1210/jcem.87.8.9998
Source DB: PubMed Journal: J Clin Endocrinol Metab ISSN: 0021-972X Impact factor: 5.958