Abrams, M T <br/><br/>
Molecular-neurobehavioral associations in females with the fragile X full mutation.  [electronic resource] 

 -  American journal of medical genetics  Jul 1994 
 - 317-27 p.  digital 
<br/><br/> Publication Type: Journal Article; Research Support, U.S. Gov't, P.H.S. 
<br/><br/><label>ISSN: </label>0148-7299 
<br/><br/><label>Standard No.: </label>10.1002/ajmg.1320510407  doi 
<br/><br/><label>Subjects--Topical Terms: </label><br/>Adolescent<br/>Adult<br/>Child<br/>Child, Preschool<br/>DNA--metabolism<br/>Dinucleoside Phosphates--metabolism<br/>Dosage Compensation, Genetic<br/>Female<br/>Fragile X Syndrome--complications<br/>Gene Dosage<br/>Heterozygote<br/>Humans<br/>Intelligence--genetics<br/>Intelligence Tests<br/>Mental Disorders--etiology<br/>Methylation<br/>Mutation<br/>Neuropsychological Tests<br/>Phenotype<br/>Regression Analysis<br/>Repetitive Sequences, Nucleic Acid<br/>Risk Assessment<br/>Schizotypal Personality Disorder--etiology