Chacon-Camacho, Oscar F <br/><br/>
Expansion of the phenotypic spectrum and description of molecular findings in a cohort of patients with oculocutaneous mosaic RASopathies.  [electronic resource] 

 -  Molecular genetics & genomic medicine  05 2019 
 - e625 p.  digital 
<br/><br/> Publication Type: Journal Article 
<br/><br/><label>ISSN: </label>2324-9269 
<br/><br/><label>Standard No.: </label>10.1002/mgg3.625  doi 
<br/><br/><label>Subjects--Topical Terms: </label><br/>Dermoid Cyst--genetics<br/>Ectodermal Dysplasia--genetics<br/>Eye Diseases--genetics<br/>GTP Phosphohydrolases--genetics<br/>Humans<br/>Lipomatosis--genetics<br/>Membrane Proteins--genetics<br/>Mosaicism<br/>Neurocutaneous Syndromes--genetics<br/>Nevus, Sebaceous of Jadassohn--genetics<br/>Phenotype<br/>Proto-Oncogene Proteins p21(ras)--genetics<br/>Receptor, Fibroblast Growth Factor, Type 1--genetics