Baralle, Diana <br/><br/>
Different mutations in the NF1 gene are associated with Neurofibromatosis-Noonan syndrome (NFNS).  [electronic resource] 

 -  American journal of medical genetics. Part A  May 2003 
 - 1-8 p.  digital 
<br/><br/> Publication Type: Case Reports; Journal Article; Research Support, Non-U.S. Gov't 
<br/><br/><label>ISSN: </label>1552-4825 
<br/><br/><label>Standard No.: </label>10.1002/ajmg.a.20023  doi 
<br/><br/><label>Subjects--Topical Terms: </label><br/>Adolescent<br/>Adult<br/>Child<br/>DNA Mutational Analysis<br/>Genes, Neurofibromatosis 1<br/>Humans<br/>Intracellular Signaling Peptides and Proteins<br/>Male<br/>Neurofibromatoses--genetics<br/>Noonan Syndrome--genetics<br/>Protein Tyrosine Phosphatase, Non-Receptor Type 1<br/>Protein Tyrosine Phosphatase, Non-Receptor Type 11<br/>Protein Tyrosine Phosphatases--genetics