Bebbington, Ami <br/><br/>
The phenotype associated with a large deletion on MECP2.  [electronic resource] 

 -  European journal of human genetics : EJHG  Sep 2012 
 - 921-7 p.  digital 
<br/><br/> Publication Type: Journal Article; Research Support, N.I.H., Extramural; Research Support, Non-U.S. Gov't 
<br/><br/><label>ISSN: </label>1476-5438 
<br/><br/><label>Standard No.: </label>10.1038/ejhg.2012.34  doi 
<br/><br/><label>Subjects--Topical Terms: </label><br/>Adolescent<br/>Adult<br/>Age of Onset<br/>Australia--epidemiology<br/>Base Sequence<br/>Child<br/>Child, Preschool<br/>Female<br/>Genetic Association Studies<br/>Genotype<br/>Humans<br/>Infant<br/>Male<br/>Methyl-CpG-Binding Protein 2--genetics<br/>Middle Aged<br/>Molecular Sequence Data<br/>Multiplex Polymerase Chain Reaction<br/>Phenotype<br/>Rett Syndrome--diagnosis<br/>Sequence Deletion<br/>Severity of Illness Index<br/>Surveys and Questionnaires