The nature of the spatial deficit in young females with Fragile-X syndrome: A neuropsychological and molecular perspective

Neuropsychologia

Volumn 36, Issue 11, 1998, Pages 1239-1246

  Cornish, K M ^a   Munir, F ^a   Cross, G ^b  

^a Medical School   (United Kingdom)

^b NOTTINGHAM CITY HOSPITAL   (United Kingdom)

Author keywords

[No Author keywords available]

Indexed keywords

ADOLESCENT; ADULT; ARTICLE; CLINICAL ARTICLE; CLINICAL FEATURE; DEPTH PERCEPTION; DISEASE CARRIER; DNA DETERMINATION; FEMALE; FRAGILE X SYNDROME; GENE MUTATION; GENETIC TRANSCRIPTION; HUMAN; INTELLIGENCE; MENTAL DEFICIENCY; PHENOTYPE; SCHOOL CHILD; SPATIAL MEMORY;

ADOLESCENT; CHILD; COGNITION DISORDERS; DEVELOPMENTAL DISABILITIES; FEMALE; FRAGILE X MENTAL RETARDATION PROTEIN; FRAGILE X SYNDROME; HUMANS; INTELLIGENCE; LEARNING DISORDERS; MULTIVARIATE ANALYSIS; NERVE TISSUE PROTEINS; NEUROPSYCHOLOGICAL TESTS; REGRESSION ANALYSIS; RNA-BINDING PROTEINS; SPACE PERCEPTION; TRINUCLEOTIDE REPEATS; X CHROMOSOME;

EID: 0031790762     PISSN: 00283932     EISSN: None     Source Type: Journal    
DOI: 10.1016/S0028-3932(97)00162-0     Document Type: Article

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