Clinical variability and novel neurodevelopmental findings in 49, XXXXY syndrome

American Journal of Medical Genetics, Part A

Volumn 152, Issue 6, 2010, Pages 1523-1530

  Gropman, Andrea L ^a,b   Rogol, Alan ^c,d   Fennoy, Ilene ^e   Sadeghin, Teresa ^f   Sinn, Stephanie ^f   Jameson, Robert ^f   Mitchell, Francine ^f   Clabaugh, Jaye ^f   Lutz Armstrong, Margaret ^f   Samango Sprouse, Carole A ^b,f  

^a CHILDREN'S NATIONAL MEDICAL CENTER   (United States)

^b GEORGE WASHINGTON UNIVERSITY   (United States)

^c UNIVERSITY OF VIRGINIA   (United States)

^d INDIANA UNIVERSITY SCHOOL OF MEDICINE   (United States)

^e New York Presbyterian Hospital Columbia University Medical Center   (United States)

^f Neurodevelopmental Diagnostic Center for Young Children   (United States)

Author keywords

Chromosome; Dyspraxia; Klinefelter; XXXXY

Indexed keywords

49 XXXXY SYDROME; ARTICLE; CHILD; CLINICAL FEATURE; COGNITION; DYSPRAXIA; HUMAN; KLINEFELTER SYNDROME; MALE; NERVOUS SYSTEM DEVELOPMENT; PHENOTYPE; PRESCHOOL CHILD; PRIORITY JOURNAL; SCHOOL CHILD; SEX CHROMOSOME ABERRATION;

ADOLESCENT; ANEUPLOIDY; CHILD; CHILD DEVELOPMENT; CHILD, PRESCHOOL; CHROMOSOMES, HUMAN, X; CHROMOSOMES, HUMAN, Y; COGNITION; HUMANS; INFANT; KLINEFELTER SYNDROME; MALE; PSYCHOMOTOR DISORDERS; SYNDROME;

EID: 77952769435     PISSN: 15524825     EISSN: 15524833     Source Type: Journal    
DOI: 10.1002/ajmg.a.33307     Document Type: Article

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