Petrof, Gabriela <br/><br/>
Mutations in GRHL2 result in an autosomal-recessive ectodermal Dysplasia syndrome.  [electronic resource] 

 -  American journal of human genetics  Sep 2014 
 - 308-14 p.  digital 
<br/><br/> Publication Type: Journal Article; Research Support, Non-U.S. Gov't 
<br/><br/><label>ISSN: </label>1537-6605 
<br/><br/><label>Standard No.: </label>10.1016/j.ajhg.2014.08.001  doi 
<br/><br/><label>Subjects--Topical Terms: </label><br/>Blotting, Western<br/>Child<br/>Cleft Palate--genetics<br/>DNA-Binding Proteins--genetics<br/>Ectodermal Dysplasia--genetics<br/>Exons--genetics<br/>Female<br/>Genes, Recessive--genetics<br/>Humans<br/>Intellectual Disability--genetics<br/>Male<br/>Mutation--genetics<br/>Pedigree<br/>Phenotype<br/>RNA, Messenger--genetics<br/>Real-Time Polymerase Chain Reaction<br/>Reverse Transcriptase Polymerase Chain Reaction<br/>Skin--metabolism<br/>Syndactyly--genetics<br/>Syndrome<br/>Transcription Factors--genetics