Neurobehavioral phenotype in carriers of the fragile X premutation

American Journal of Medical Genetics

Volumn 103, Issue 4, 2001, Pages 314-319

  Johnston, Cindy ^a   Eliez, Stephan ^a   Dyer Friedman, Jennifer ^b   Hessl, David ^b   Glaser, Bronwyn ^c   Blasey, Christine ^c   Taylor, Annette ^d   Reiss, Allan ^a  

^a STANFORD UNIVERSITY SCHOOL OF MEDICINE   (United States)

^b Kimball Genetics Inc   (United States)

^c Department of Psychiatry and Behavioral Sciences ^*  (United States)

^d STANFORD UNIVERSITY   (United States)

Author keywords

Allele size; Cognition; Fragile X syndrome; Premutation; Psychological symptoms

Indexed keywords

DNA; TRINUCLEOTIDE;

ADULT; AGE; ALLELE; ARTICLE; CLINICAL FEATURE; COGNITION; CONTROLLED STUDY; DEPRESSION; FEMALE; FOLLOW UP; FRAGILE X SYNDROME; HETEROZYGOTE; HUMAN; HUMAN TISSUE; INTELLIGENCE QUOTIENT; MAJOR CLINICAL STUDY; PHENOTYPE; PRIORITY JOURNAL; QUESTIONNAIRE; TRINUCLEOTIDE REPEAT;

ADULT; COGNITION; FEMALE; FRAGILE X MENTAL RETARDATION PROTEIN; FRAGILE X SYNDROME; HOMOZYGOTE; HUMANS; MEMORY; MIDDLE AGED; MUTATION; NERVE TISSUE PROTEINS; NEUROPSYCHOLOGICAL TESTS; NUCLEAR FAMILY; PEDIGREE; RNA-BINDING PROTEINS; SPEECH; TRINUCLEOTIDE REPEATS; WECHSLER SCALES;

EID: 0035500835     PISSN: 01487299     EISSN: None     Source Type: Journal    
DOI: 10.1002/ajmg.1561     Document Type: Article

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