Pawlowska, Elzbieta <br/><br/>
Mutations in the human homeobox MSX1 gene in the congenital lack of permanent teeth.  [electronic resource] 

 -  The Tohoku journal of experimental medicine  Apr 2009 
 - 307-12 p.  digital 
<br/><br/> Publication Type: Journal Article; Research Support, Non-U.S. Gov't 
<br/><br/><label>ISSN: </label>1349-3329 
<br/><br/><label>Standard No.: </label>10.1620/tjem.217.307  doi 
<br/><br/><label>Subjects--Topical Terms: </label><br/>Adolescent<br/>Anodontia--diagnostic imaging<br/>Base Sequence<br/>Child<br/>DNA Primers--genetics<br/>Female<br/>Gene Components<br/>Genetic Predisposition to Disease--genetics<br/>Humans<br/>MSX1 Transcription Factor--genetics<br/>Male<br/>Molecular Sequence Data<br/>Radiography<br/>Sequence Analysis, DNA<br/>Sequence Deletion