A controlled study of longitudinal IQ changes in females and males with fragile X syndrome

American Journal of Medical Genetics

Volumn 64, Issue 2, 1996, Pages 350-355

  Wright Talamante, Cara ^a   Cheema, Asma ^b   Riddle, Jeannette E ^b   Luckey, Dennis W ^c   Taylor, Annette K ^d   Hagerman, Randi J ^b,c  

^a PHOENIX CHILDREN'S HOSPITAL   (United States)

^b CHILDREN S HOSPITAL   (United States)

^c UNIVERSITY OF COLORADO   (United States)

^d Kimball Genetics   (United States)

Author keywords

fragile X; IQ follow up; learning disabilities; methylation; molecular clinical correlations

Indexed keywords

ADOLESCENT; ARTICLE; CHILD; CHILD DEVELOPMENT; CLINICAL ARTICLE; CONTROLLED STUDY; FEMALE; FOLLOW UP; FRAGILE X SYNDROME; GENETIC ANALYSIS; HUMAN; INFANT; INTELLIGENCE QUOTIENT; LEARNING DISORDER; LONGITUDINAL STUDY; MALE; METHYLATION; MOLECULAR GENETICS; PRIORITY JOURNAL;

ADOLESCENT; CASE-CONTROL STUDIES; CHILD; DNA METHYLATION; FEMALE; FRAGILE X SYNDROME; HUMANS; INTELLIGENCE; LONGITUDINAL STUDIES; MALE; MOSAICISM; REFERENCE VALUES; SEX CHARACTERISTICS;

EID: 0029896929     PISSN: 01487299     EISSN: None     Source Type: Journal    
DOI: 10.1002/(SICI)1096-8628(19960809)64:2<350::AID-AJMG23>3.0.CO;2-D     Document Type: Article

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