Craniofacial cephalometric morphology in children with CATCH 22 syndrome

Orthodontics and Craniofacial Research

Volumn 9, Issue 4, 2006, Pages 186-192

  Vaara, Arja Heliö ^a   Hurmerinta, Kirsti ^a  

^a HELSINKI UNIVERSITY CENTRAL HOSPITAL   (Finland)

Author keywords

22q11 deletion; CATCH 22; Cephalometrics; Craniofacial morphology; Pharynx

Indexed keywords

ARTICLE; CASE CONTROL STUDY; CEPHALOMETRY; CERVICAL SPINE; CHILD; CHROMOSOME 22; CHROMOSOME DELETION; CONGENITAL HEART MALFORMATION; CONGENITAL MALFORMATION; CRANIOFACIAL MALFORMATION; FACE; FACIES; FEMALE; FLUORESCENCE IN SITU HYBRIDIZATION; HUMAN; MALE; MENTAL DEFICIENCY; MULTIPLE MALFORMATION SYNDROME; PATHOLOGY; PHARYNX; PRESCHOOL CHILD; RETROSPECTIVE STUDY; SYNDROME;

ABNORMALITIES, MULTIPLE; CASE-CONTROL STUDIES; CEPHALOMETRY; CERVICAL VERTEBRAE; CHILD; CHILD, PRESCHOOL; CHROMOSOME DELETION; CHROMOSOMES, HUMAN, PAIR 22; CRANIOFACIAL ABNORMALITIES; FACE; FACIES; FEMALE; HEART DEFECTS, CONGENITAL; HUMANS; IN SITU HYBRIDIZATION, FLUORESCENCE; MALE; MENTAL RETARDATION; PHARYNX; RETROSPECTIVE STUDIES; SYNDROME;

EID: 39049178683     PISSN: 16016335     EISSN: 16016343     Source Type: Journal    
DOI: 10.1111/j.1601-6343.2006.00373.x     Document Type: Article

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