Kneitel, Anna W <br/><br/>
A Novel Mutation on RAF1 in Association with Fetal Findings Suggestive of Noonan Syndrome.  [electronic resource] 

 -  Fetal and pediatric pathology  2015 
 - 361-4 p.  digital 
<br/><br/> Publication Type: Case Reports; Journal Article 
<br/><br/><label>ISSN: </label>1551-3823 
<br/><br/><label>Standard No.: </label>10.3109/15513815.2015.1087609  doi 
<br/><br/><label>Subjects--Topical Terms: </label><br/>Female<br/>Fetus<br/>Humans<br/>Male<br/>Mutation, Missense<br/>Noonan Syndrome--genetics<br/>Pregnancy<br/>Prenatal Diagnosis<br/>Proto-Oncogene Proteins c-raf--genetics