Electrocardiography in Noonan syndrome PTPN11 gene mutation--phenotype characterization. [electronic resource]
- American journal of medical genetics. Part A Feb 2008
- 350-3 p. digital
Publication Type: Journal Article
1552-4833
10.1002/ajmg.a.32140 doi
Child, Preschool Cross-Sectional Studies Electrocardiography Female Heart Defects, Congenital--genetics Humans Infant Male Mutation Noonan Syndrome--genetics Phenotype Protein Tyrosine Phosphatase, Non-Receptor Type 11--genetics