Madson, Justin G <br/><br/>
Multiple or familial café-au-lait spots is neurofibromatosis type 6: clarification of a diagnosis.  [electronic resource] 

 -  Dermatology online journal  May 2012 
 - 4 p.  digital 
<br/><br/> Publication Type: Journal Article 
<br/><br/><label>ISSN: </label>1087-2108 
<br/><br/><label>Subjects--Topical Terms: </label><br/>Cafe-au-Lait Spots--diagnosis<br/>Child, Preschool<br/>Chromogranins<br/>Diagnosis, Differential<br/>Diagnostic Errors<br/>Fibrous Dysplasia, Polyostotic--diagnosis<br/>GTP-Binding Protein alpha Subunits, Gs--genetics<br/>Genes, Neurofibromatosis 1<br/>Genes, Neurofibromatosis 2<br/>Humans<br/>Infant<br/>Infant, Newborn<br/>Mutation<br/>Neurofibromatoses--diagnosis<br/>Neurofibromatosis 1--diagnosis<br/>Neurofibromatosis 2--diagnosis<br/>Terminology as Topic