Croonen, Ellen A <br/><br/>
Patient with a neurofibromatosis type 1 mutation but a clinical diagnosis of Noonan syndrome.  [electronic resource] 

 -  Clinical dysmorphology  Oct 2012 
 - 212-214 p.  digital 
<br/><br/> Publication Type: Case Reports; Journal Article 
<br/><br/><label>ISSN: </label>1473-5717 
<br/><br/><label>Standard No.: </label>10.1097/MCD.0b013e3283557231  doi 
<br/><br/><label>Subjects--Topical Terms: </label><br/>Child<br/>Child, Preschool<br/>Diagnosis, Differential<br/>Humans<br/>Infant<br/>Infant, Newborn<br/>Mutation--genetics<br/>Neurofibromatosis 1--genetics<br/>Noonan Syndrome--diagnosis