Dental developmental disturbances in 50 individuals with the 22q11.2 deletion syndrome; Relation to medical conditions?

Acta Odontologica Scandinavica

Volumn 70, Issue 3, 2012, Pages 194-201

  Nordgarden, Hilde ^a   Lima, Kari ^b,c,d   Skogedal, Nina ^a   Følling, Ivar ^b   Storhaug, Kari ^a   Abrahamsen, Tore G ^c,d  

^a LOVISENBERG DIAKONALE HOSPITAL   (Norway)

^b Akerhus University Hospital   (Norway)

^c UNIVERSITY OF OSLO   (Norway)

^d OSLO UNIVERSITY HOSPITAL   (Norway)

Author keywords

22q11 deletion syndrome; Amelogenesis; Enamel hypomineralization; Enamel hypoplasias

Indexed keywords

CALCIUM; PARATHYROID HORMONE;

ADOLESCENT; ADULT; ARTICLE; BLOOD; CHILD; CONGENITAL MALFORMATION; DENTAL PROCEDURE; DENTITION; DIGEORGE SYNDROME; ENAMEL; ENAMEL HYPOPLASIA; FEMALE; GENETICS; HUMAN; HYPODONTIA; INFANT; MALE; PRESCHOOL CHILD; TOOTH DISEASE; TOOTH MALFORMATION; VELOCARDIOFACIAL SYNDROME;

ADOLESCENT; ADULT; ANODONTIA; CALCIUM; CHILD; CHILD, PRESCHOOL; DENTAL CARE FOR CHRONICALLY ILL; DENTAL ENAMEL; DENTAL ENAMEL HYPOPLASIA; DENTITION, PERMANENT; DENTITION, PRIMARY; DIGEORGE SYNDROME; FEMALE; HUMANS; INFANT; MALE; PARATHYROID HORMONE; TOOTH ABNORMALITIES; TOOTH DEMINERALIZATION; YOUNG ADULT;

EID: 84859919847     PISSN: 00016357     EISSN: 15023850     Source Type: Journal    
DOI: 10.3109/00016357.2011.629624     Document Type: Article

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