Poulter, James A <br/><br/>
Whole-exome sequencing, without prior linkage, identifies a mutation in LAMB3 as a cause of dominant hypoplastic amelogenesis imperfecta.  [electronic resource] 

 -  European journal of human genetics : EJHG  Jan 2014 
 - 132-5 p.  digital 
<br/><br/> Publication Type: Journal Article; Research Support, Non-U.S. Gov't 
<br/><br/><label>ISSN: </label>1476-5438 
<br/><br/><label>Standard No.: </label>10.1038/ejhg.2013.76  doi 
<br/><br/><label>Subjects--Topical Terms: </label><br/>Amelogenesis Imperfecta--etiology<br/>Cell Adhesion Molecules--genetics<br/>Epidermolysis Bullosa, Junctional--genetics<br/>Exome<br/>Female<br/>Frameshift Mutation<br/>Genetic Linkage<br/>High-Throughput Nucleotide Sequencing<br/>Humans<br/>Male<br/>Pedigree<br/>Kalinin