Mansur, Ayse Tulin <br/><br/>
Marie Unna hereditary hypotrichosis: a Turkish family with loss of eyebrows and a U2HR mutation.  [electronic resource] 

 -  American journal of medical genetics. Part A  Oct 2010 
 - 2628-33 p.  digital 
<br/><br/> Publication Type: Case Reports; Journal Article; Research Support, Non-U.S. Gov't 
<br/><br/><label>ISSN: </label>1552-4833 
<br/><br/><label>Standard No.: </label>10.1002/ajmg.a.33649  doi 
<br/><br/><label>Subjects--Topical Terms: </label><br/>Adolescent<br/>Diagnosis, Differential<br/>Eyebrows--abnormalities<br/>Family<br/>Female<br/>Genetic Markers<br/>Hair--abnormalities<br/>Hair Diseases--genetics<br/>Humans<br/>Hypotrichosis--diagnosis<br/>Male<br/>Microscopy, Electron, Scanning<br/>Pedigree<br/>Transcription Factors--genetics<br/>Turkey