Fragile X syndrome and selective mutism

American Journal of Medical Genetics

Volumn 83, Issue 4, 1999, Pages 313-317

  Hagerman, Randi J ^a,b,c   Hills, J ^a   Scharfenaker, S ^a   Lewis, H ^b  

^a CHILDREN S HOSPITAL   (United States)

^b UNIVERSITY OF COLORADO   (United States)

^c Child Development Unit B140   (United States)

Author keywords

FMR1 mutation; Fragile X syndrome; Selective mutism

Indexed keywords

FLUOXETINE;

ARTICLE; CASE REPORT; CHILD BEHAVIOR; CLINICAL FEATURE; DISEASE ASSOCIATION; DISEASE COURSE; FAMILY HISTORY; FEMALE; FRAGILE X SYNDROME; HETEROZYGOTE; HUMAN; LANGUAGE TEST; MUTISM; PRIORITY JOURNAL; PSYCHOLOGIC ASSESSMENT; PSYCHOTHERAPY; SCHOOL CHILD; TREATMENT OUTCOME;

CHILD; FEMALE; FRAGILE X MENTAL RETARDATION PROTEIN; FRAGILE X SYNDROME; HUMANS; MUTISM; NERVE TISSUE PROTEINS; RNA-BINDING PROTEINS;

EID: 0033515582     PISSN: 01487299     EISSN: None     Source Type: Journal    
DOI: 10.1002/(SICI)1096-8628(19990402)83:4<313::AID-AJMG15>3.0.CO;2-F     Document Type: Article

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