Facial features in children with the 22q11 deletion syndrome

Acta Paediatrica, International Journal of Paediatrics

Volumn 97, Issue 8, 2008, Pages 1113-1117

  Oskarsdottir S ^a,b   Holmberg, E ^a   Fasth, A ^a   Stromland K ^a  

^a UNIVERSITY OF GOTHENBURG   (Sweden)

^b QUEEN SILVIA CHILDREN'S HOSPITAL   (Sweden)

Author keywords

22q11 deletion; DiGeorge syndrome; Dysmorphology; Facial features; Velocardiofacial syndrome

Indexed keywords

ADOLESCENT; ADULT; ARTICLE; CHILD; CHROMOSOME 22Q; CHROMOSOME DELETION; EAR; FACIES; FEMALE; HUMAN; INFANT; MAJOR CLINICAL STUDY; MALE; NEWBORN; NOSE APEX; PHOTOGRAPHY; PRESCHOOL CHILD; PRIORITY JOURNAL; SCHOOL CHILD; ZYGOMA; CHROMOSOME 22; CONGENITAL MALFORMATION; EXTERNAL EAR; EYE; FACE; FACIAL EXPRESSION; GENETICS; HISTOLOGY; NOSE; PHENOTYPE;

CHILD; CHILD, PRESCHOOL; CHROMOSOME DELETION; CHROMOSOMES, HUMAN, PAIR 22; EAR, EXTERNAL; EYE; FACE; FACIAL EXPRESSION; FEMALE; HUMANS; INFANT; MALE; NOSE; PHENOTYPE;

EID: 63849124037     PISSN: 08035253     EISSN: 16512227     Source Type: Journal    
DOI: 10.1111/j.1651-2227.2008.00858.x     Document Type: Article

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