Klaassens, M <br/><br/>
Unique skin changes in a case of Albright hereditary osteodystrophy caused by a rare GNAS1 mutation.  [electronic resource] 

 -  The British journal of dermatology  Mar 2010 
 - 690-4 p.  digital 
<br/><br/> Publication Type: Case Reports; Journal Article; Research Support, Non-U.S. Gov't 
<br/><br/><label>ISSN: </label>1365-2133 
<br/><br/><label>Standard No.: </label>10.1111/j.1365-2133.2009.09543.x  doi 
<br/><br/><label>Subjects--Topical Terms: </label><br/>Chromogranins<br/>Fibrous Dysplasia, Polyostotic--genetics<br/>GTP-Binding Protein alpha Subunits, Gs--genetics<br/>Humans<br/>Infant<br/>Male<br/>Mutation--genetics<br/>Pedigree<br/>Pseudohypoparathyroidism--genetics<br/>Skin--pathology