Twigg, Stephen R F <br/><br/>
Frontorhiny, a distinctive presentation of frontonasal dysplasia caused by recessive mutations in the ALX3 homeobox gene.  [electronic resource] 

 -  American journal of human genetics  May 2009 
 - 698-705 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.2009.04.009  doi 
<br/><br/><label>Subjects--Topical Terms: </label><br/>Child<br/>Chromosomes, Human, Pair 1--genetics<br/>Craniofacial Abnormalities--genetics<br/>Homeodomain Proteins--genetics<br/>Humans<br/>Infant, Newborn<br/>Mutation<br/>Nasal Bone--abnormalities