Ishii, T <br/><br/>
The role of different X-inactivation pattern on the variable clinical phenotype with Rett syndrome.  [electronic resource] 

 -  Brain & development  Dec 2001 
 - S161-4 p.  digital 
<br/><br/> Publication Type: Journal Article 
<br/><br/><label>ISSN: </label>0387-7604 
<br/><br/><label>Standard No.: </label>10.1016/s0387-7604(01)00344-8  doi 
<br/><br/><label>Subjects--Topical Terms: </label><br/>Adult<br/>Allelic Imbalance--genetics<br/>Amino Acid Sequence--genetics<br/>Base Sequence--genetics<br/>Chromosomal Proteins, Non-Histone<br/>DNA Mutational Analysis<br/>DNA-Binding Proteins--genetics<br/>Disease Progression<br/>Dosage Compensation, Genetic<br/>Female<br/>Humans<br/>Male<br/>Methyl-CpG-Binding Protein 2<br/>Mutation--genetics<br/>Pedigree<br/>Phenotype<br/>Point Mutation--genetics<br/>Repressor Proteins<br/>Rett Syndrome--genetics<br/>Twins, Monozygotic--genetics