Van Geel, M <br/><br/>
Phenotypic variability associated with WNT10A nonsense mutations.  [electronic resource] 

 -  The British journal of dermatology  Jun 2010 
 - 1403-6 p.  digital 
<br/><br/> Publication Type: Case Reports; Letter; Research Support, Non-U.S. Gov't 
<br/><br/><label>ISSN: </label>1365-2133 
<br/><br/><label>Standard No.: </label>10.1111/j.1365-2133.2010.09703.x  doi 
<br/><br/><label>Subjects--Topical Terms: </label><br/>Adult<br/>Ectodermal Dysplasia--genetics<br/>Female<br/>Hair Diseases--genetics<br/>Hair Follicle--abnormalities<br/>Humans<br/>Male<br/>Middle Aged<br/>Mutation, Missense--genetics<br/>Phenotype<br/>Sequence Analysis, DNA<br/>Wnt Proteins--genetics<br/>Young Adult