Evidence Report: Genetic and metabolic testing on children with global developmental delay: Report of the quality standards Subcommittee of the American Academy of Neurology and the Practice Committee of the Child Neurology Society

Neurology

Volumn 77, Issue 17, 2011, Pages 1629-1635

  Michelson, D J ^a   Shevell, M I ^b   Sherr, E H ^c   Moeschler, J B ^d   Gropman, A L ^e   Ashwal, S ^a  

^a LOMA LINDA UNIVERSITY   (United States)

^b MCGILL UNIVERSITY   (Canada)

^c UNIVERSITY OF CALIFORNIA   (United States)

^d DARTMOUTH HITCHCOCK MEDICAL CENTER   (United States)

^e GEORGE WASHINGTON UNIVERSITY SCHOOL OF MEDICINE AND HEALTH SCIENCES   (United States)

Author keywords

[No Author keywords available]

Indexed keywords

CREATINE; FRAGILE X MENTAL RETARDATION PROTEIN;

ARTICLE; CHROMOSOME G BAND; DEVELOPMENTAL DISORDER; DIAGNOSTIC PROCEDURE; DISEASE SEVERITY; FAMILY HISTORY; FLUORESCENCE IN SITU HYBRIDIZATION; GENETIC ANALYSIS; GENETIC ASSOCIATION; GLYCOSYLATION; HUMAN; INTELLECTUAL IMPAIRMENT; LABORATORY TEST; MEDICAL SOCIETY; METABOLIC PARAMETERS; MICROARRAY ANALYSIS; PRIORITY JOURNAL; QUALITY CONTROL; SYSTEMATIC REVIEW;

EID: 82955235679     PISSN: 00283878     EISSN: 1526632X     Source Type: Journal    
DOI: 10.1212/WNL.0b013e3182345896     Document Type: Article

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