Chassaing, Nicolas <br/><br/>
Generalized epidermolytic hyperkeratosis in two unrelated children from parents with localized linear form, and prenatal diagnosis.  [electronic resource] 

 -  The Journal of investigative dermatology  Dec 2006 
 - 2715-7 p.  digital 
<br/><br/> Publication Type: Letter; Research Support, Non-U.S. Gov't 
<br/><br/><label>ISSN: </label>1523-1747 
<br/><br/><label>Standard No.: </label>10.1038/sj.jid.5700553  doi 
<br/><br/><label>Subjects--Topical Terms: </label><br/>Adult<br/>DNA Mutational Analysis<br/>Female<br/>Glutamic Acid<br/>Humans<br/>Hyperkeratosis, Epidermolytic--diagnosis<br/>Infant, Newborn<br/>Isoleucine<br/>Keratin-1--genetics<br/>Keratin-10--genetics<br/>Lysine<br/>Mutation<br/>Phenylalanine<br/>Prenatal Diagnosis<br/>Skin--pathology