Hoffbuhr, K <br/><br/>
MeCP2 mutations in children with and without the phenotype of Rett syndrome.  [electronic resource] 

 -  Neurology  Jun 2001 
 - 1486-95 p.  digital 
<br/><br/> Publication Type: Journal Article; Research Support, Non-U.S. Gov't; Research Support, U.S. Gov't, P.H.S. 
<br/><br/><label>ISSN: </label>0028-3878 
<br/><br/><label>Standard No.: </label>10.1212/wnl.56.11.1486  doi 
<br/><br/><label>Subjects--Topical Terms: </label><br/>Adolescent<br/>Adult<br/>Child<br/>Child, Preschool<br/>Chromosomal Proteins, Non-Histone<br/>DNA Mutational Analysis<br/>DNA-Binding Proteins--genetics<br/>Dosage Compensation, Genetic<br/>Female<br/>Gene Deletion<br/>Gene Rearrangement<br/>Genotype<br/>Humans<br/>Male<br/>Methyl-CpG-Binding Protein 2<br/>Phenotype<br/>Point Mutation<br/>Repressor Proteins<br/>Rett Syndrome--genetics<br/>Severity of Illness Index