22q11.2DS deletion syndrome: Developmental milestones in infants and toddlers

Journal of Developmental and Behavioral Pediatrics

Volumn 28, Issue 2, 2007, Pages 119-124

  Roizen, Nancy J ^a   Antshel, Kevin M ^b   Fremont, Wanda ^b   Abdulsabur, Nuria ^b   Higgins, Anne Marie ^b   Shprintzen, Robert J ^b   Kates, Wendy R ^b,c,d,e  

^a LERNER RESEARCH INSTITUTE   (United States)

^b State University of New York Upstate Medical University: College of Medicine   (United States)

^c STATE UNIVERSITY OF NEW YORK   (United States)

^d JOHNS HOPKINS UNIVERSITY SCHOOL OF MEDICINE   (United States)

^e NONE   (United States)

Author keywords

22q11.2 deletion syndrome; Conotruncal anomalies face syndrome; Development; DiGeorge syndrome; Milestones; Shprintzen syndrome; Velocardiofacial syndrome

Indexed keywords

ADOLESCENT; ARTICLE; CHILD DEVELOPMENT; CHROMOSOME 22Q; CHROMOSOME DELETION; COGNITION; COMMUNITY; CONTROL GROUP; CONTROLLED STUDY; DEVELOPMENTAL DISORDER; FEMALE; HUMAN; INTELLECT; LANGUAGE ABILITY; MAJOR CLINICAL STUDY; MALE; MOTOR PERFORMANCE; PARENT; PREDICTION; PRIORITY JOURNAL; RETROSPECTIVE STUDY; SCHOOL CHILD; SCORING SYSTEM; SIBLING; SOCIAL ADAPTATION; TODDLER; WECHSLER INTELLIGENCE SCALE;

AGE FACTORS; CHILD, PRESCHOOL; CHROMOSOME DELETION; CHROMOSOMES, HUMAN, PAIR 22; DEVELOPMENTAL DISABILITIES; DIGEORGE SYNDROME; FEMALE; HUMANS; INFANT; LANGUAGE DEVELOPMENT DISORDERS; LEARNING DISORDERS; MALE; MENTAL RETARDATION; MOTOR SKILLS; PSYCHOMOTOR DISORDERS; REFERENCE VALUES; WECHSLER SCALES;

EID: 34247279194     PISSN: 0196206X     EISSN: None     Source Type: Journal    
DOI: 10.1097/01.DBP.0000267554.96081.12     Document Type: Article

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