Craniofacial dysmorphism and developmental disorders among children with chromosomal microdeletions and duplications of unknown significance

Journal of Developmental and Behavioral Pediatrics

Volumn 32, Issue 8, 2011, Pages 600-604

  Gannon, William T ^a   Martinez, Jose E ^b   Anderson, Stephanie J ^a   Swingle, Hanes M ^a,b  

^a Division of Developmental Behavioral Pediatrics   (United States)

^b UNIVERSITY OF SOUTH ALABAMA COLLEGE OF MEDICINE   (United States)

Author keywords

array comparative genomic hybridization; autism spectrum disorders; developmental delay; dysmorphology

Indexed keywords

ARTICLE; AUTISM; CHILD; CHROMOSOME DELETION; CHROMOSOME DUPLICATION; COMORBIDITY; CRANIOFACIAL MALFORMATION; DEVELOPMENTAL DISORDER; DNA MICROARRAY; FEMALE; GENETIC PREDISPOSITION; GENETICS; HUMAN; MALE; METHODOLOGY; PHENOTYPE; PRESCHOOL CHILD; PSYCHOLOGICAL ASPECT;

AUTISTIC DISORDER; CHILD; CHILD, PRESCHOOL; CHROMOSOME DELETION; CHROMOSOME DUPLICATION; COMORBIDITY; CRANIOFACIAL ABNORMALITIES; DEVELOPMENTAL DISABILITIES; FEMALE; GENETIC PREDISPOSITION TO DISEASE; HUMANS; MALE; OLIGONUCLEOTIDE ARRAY SEQUENCE ANALYSIS; PHENOTYPE;

EID: 80053579802     PISSN: 0196206X     EISSN: None     Source Type: Journal    
DOI: 10.1097/DBP.0b013e31823299d6     Document Type: Article

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