Stuart, Helen M <br/><br/>
LRIG2 mutations cause urofacial syndrome.  [electronic resource] 

 -  American journal of human genetics  Feb 2013 
 - 259-64 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.2012.12.002  doi 
<br/><br/><label>Subjects--Topical Terms: </label><br/>Base Sequence<br/>Child<br/>Child, Preschool<br/>DNA Mutational Analysis<br/>Facies<br/>Family<br/>Female<br/>Humans<br/>Immunohistochemistry<br/>Infant<br/>Male<br/>Membrane Glycoproteins--genetics<br/>Molecular Sequence Data<br/>Mutation--genetics<br/>Pedigree<br/>Urinary Bladder--pathology<br/>Urinary Bladder, Neurogenic--genetics<br/>Urologic Diseases--genetics