Goizet, Cyril <br/><br/>
Molecular characterization of an 11q14.3 microdeletion associated with leukodystrophy.  [electronic resource] 

 -  European journal of human genetics : EJHG  Mar 2004 
 - 245-50 p.  digital 
<br/><br/> Publication Type: Journal Article; Research Support, Non-U.S. Gov't 
<br/><br/><label>ISSN: </label>1018-4813 
<br/><br/><label>Standard No.: </label>10.1038/sj.ejhg.5201128  doi 
<br/><br/><label>Subjects--Topical Terms: </label><br/>Cathepsin C--genetics<br/>Chromosome Deletion<br/>Chromosomes, Artificial, Bacterial--genetics<br/>Chromosomes, Human, Pair 11--genetics<br/>Contig Mapping<br/>Humans<br/>In Situ Hybridization, Fluorescence<br/>Leukodystrophy, Metachromatic--genetics<br/>Microsatellite Repeats--genetics<br/>Physical Chromosome Mapping<br/>Receptor, Metabotropic Glutamate 5<br/>Receptors, Metabotropic Glutamate--genetics