Reiss, A L <br/><br/>
Contribution of the FMR1 gene mutation to human intellectual dysfunction.  [electronic resource] 

 -  Nature genetics  Nov 1995 
 - 331-4 p.  digital 
<br/><br/> Publication Type: Journal Article; Research Support, U.S. Gov't, P.H.S. 
<br/><br/><label>ISSN: </label>1061-4036 
<br/><br/><label>Standard No.: </label>10.1038/ng1195-331  doi 
<br/><br/><label>Subjects--Topical Terms: </label><br/>Adolescent<br/>Case-Control Studies<br/>Child<br/>Dosage Compensation, Genetic<br/>Female<br/>Fragile X Mental Retardation Protein<br/>Fragile X Syndrome--genetics<br/>Humans<br/>Intellectual Disability--genetics<br/>Intelligence--genetics<br/>Intelligence Tests<br/>Mutation<br/>Nerve Tissue Proteins--genetics<br/>Parents<br/>RNA-Binding Proteins<br/>Regression Analysis<br/>Repetitive Sequences, Nucleic Acid