Donzel-Javouhey, Anne <br/><br/>
A new cohort of MECP2 mutation screening in unexplained mental retardation: careful re-evaluation is the best indicator for molecular diagnosis.  [electronic resource] 

 -  American journal of medical genetics. Part A  Jul 2006 
 - 1603-7 p.  digital 
<br/><br/> Publication Type: Letter; Research Support, Non-U.S. Gov't 
<br/><br/><label>ISSN: </label>1552-4825 
<br/><br/><label>Standard No.: </label>10.1002/ajmg.a.31314  doi 
<br/><br/><label>Subjects--Topical Terms: </label><br/>Base Sequence<br/>Cohort Studies<br/>DNA--genetics<br/>Female<br/>Genetic Testing<br/>Humans<br/>Intellectual Disability--genetics<br/>Male<br/>Methyl-CpG-Binding Protein 2--genetics<br/>Mutation<br/>Phenotype<br/>Rett Syndrome--genetics