Bertola, D R <br/><br/>
Multiple, diffuse schwannomas in a RASopathy phenotype patient with germline KRAS mutation: a causal relationship?  [electronic resource] 

 -  Clinical genetics  Jun 2012 
 - 595-7 p.  digital 
<br/><br/> Publication Type: Case Reports; Letter; Research Support, Non-U.S. Gov't 
<br/><br/><label>ISSN: </label>1399-0004 
<br/><br/><label>Standard No.: </label>10.1111/j.1399-0004.2011.01764.x  doi 
<br/><br/><label>Subjects--Topical Terms: </label><br/>Child<br/>Chromosomal Proteins, Non-Histone--genetics<br/>DNA-Binding Proteins--genetics<br/>Female<br/>Germ-Line Mutation<br/>Humans<br/>Neurilemmoma--genetics<br/>Neurofibromin 2--genetics<br/>Phenotype<br/>Proto-Oncogene Proteins--genetics<br/>Proto-Oncogene Proteins p21(ras)<br/>SMARCB1 Protein<br/>Transcription Factors--genetics<br/>Young Adult<br/>ras Proteins--genetics