Milà, M <br/><br/>
Screening for FMR1 and FMR2 mutations in 222 individuals from Spanish special schools: identification of a case of FRAXE-associated mental retardation.  [electronic resource] 

 -  Human genetics  Oct 1997 
 - 503-7 p.  digital 
<br/><br/> Publication Type: Journal Article; Research Support, Non-U.S. Gov't 
<br/><br/><label>ISSN: </label>0340-6717 
<br/><br/><label>Standard No.: </label>10.1007/s004390050542  doi 
<br/><br/><label>Subjects--Topical Terms: </label><br/>Adolescent<br/>Adult<br/>Child<br/>Child, Preschool<br/>Chromosome Fragile Sites<br/>Chromosome Fragility<br/>DNA Methylation<br/>Female<br/>Fragile X Mental Retardation Protein<br/>Fragile X Syndrome--genetics<br/>Genetic Testing<br/>Humans<br/>Male<br/>Mosaicism<br/>Mutation--genetics<br/>Nerve Tissue Proteins--genetics<br/>Nuclear Proteins<br/>Phenotype<br/>Proteins--genetics<br/>Psychotic Disorders--genetics<br/>RNA-Binding Proteins<br/>Schools<br/>Spain<br/>Trans-Activators<br/>Trinucleotide Repeats--genetics<br/>X Chromosome--genetics