Developmental disorders of the dentition: An update

American Journal of Medical Genetics, Part C: Seminars in Medical Genetics

Volumn 163, Issue 4, 2013, Pages 318-332

  Klein, Ophir D ^a,b   Oberoi, Snehlata ^c   Huysseune, Ann ^d   Hovorakova, Maria ^e   Peterka, Miroslav ^e,f   Peterkova, Renata ^e  

^a Departments of Orofacial Sciences and Pediatrics   (United States)

^b Division of Craniofacial Anomalies   (United States)

^c Center for Craniofacial Anomalies   (United States)

^d GHENT UNIVERSITY   (Belgium)

^e INSTITUTE OF EXPERIMENTAL MEDICINE   (Czech Republic)

^f CHARLES UNIVERSITY   (Czech Republic)

Author keywords

Craniofacial; Hypodontia; Mouse; Supernumerary teeth; Syndrome; Teeth; Zebrafish

Indexed keywords

AXIN; AXIN2; BONE MORPHOGENETIC PROTEIN 2; BONE MORPHOGENETIC PROTEIN 4; GLYCOSAMINOGLYCAN; HYALURONIC ACID; INTERFERON REGULATORY FACTOR 6; LYMPHOID ENHANCER FACTOR 1; SONIC HEDGEHOG PROTEIN; TRANSCRIPTION FACTOR MSX1; TRANSCRIPTION FACTOR PAX9; TRANSCRIPTION FACTOR RUNX2; TRANSFORMING GROWTH FACTOR BETA; UNCLASSIFIED DRUG; WNT PROTEIN; WNT10A PROTEIN; WNT5A PROTEIN;

ACROCEPHALOSYNDACTYLY; ANKYLOGLOSSIA; APOPTOSIS; ARTICLE; AUTOSOMAL DOMINANT INHERITANCE; CHROMOSOME; CHROMOSOME 4; CLEFT LIP; CLEFT PALATE; CLEIDOCRANIAL DYSPLASIA; DECIDUOUS TOOTH; DENTIN; DENTITION; DEVELOPMENTAL DISORDER; DOMINANT INHERITANCE; DUANE RETRACTION SYNDROME; DUBOWITZ SYNDROME; ECTODERMAL DYSPLASIA; EPITHELIUM CELL; GARDNER SYNDROME; GENETICS; HOLOPROSENCEPHALY; HUMAN; HYPODONTIA; MENKE SYNDROME; MESENCHYME; MESENCHYME CELL; MICROGNATHIA; MISSENSE MUTATION; MORPHOGENESIS; MOUTH MUCOSA; MULTIFACTORIAL INHERITANCE; MUTATION; NONHUMAN; OCULOFACIOCARDIODENTAL SYNDROME; ODONTOBLAST; ORAL FACIAL DIGITAL SYNDROME TYPE 1; PIERRE ROBIN SYNDROME; PREVALENCE; PRIORITY JOURNAL; PROGERIA; RIEGER SYNDROME; SMITH MAGENIS SYNDROME; SYNDROME CHARGE; TOOTH DEVELOPMENT; TOOTH ERUPTION; TOOTH FLORA; TOOTH MALFORMATION; TOOTH SIZE; UNILATERAL CLEFT LIP; VAN DER WOUDE SYNDROME; VELOCARDIOFACIAL SYNDROME; WEBBED NECK; X CHROMOSOME INACTIVATION; ZEBRA FISH; ANIMAL; ANTERIOR EYE SEGMENT; COMPLICATION; CYST; DYSOSTOSIS; EYE MALFORMATION; GROWTH, DEVELOPMENT AND AGING; LIP; MOUSE; MULTIPLE MALFORMATION SYNDROME; PATHOLOGY; PATHOPHYSIOLOGY; TOOTH;

DANIO RERIO;

ABNORMALITIES, MULTIPLE; ANIMALS; ANTERIOR EYE SEGMENT; CLEFT LIP; CLEFT PALATE; CYSTS; DENTITION; DEVELOPMENTAL DISABILITIES; ECTODERMAL DYSPLASIA; EYE ABNORMALITIES; HOLOPROSENCEPHALY; HUMANS; LIP; MICE; OROFACIODIGITAL SYNDROMES; TOOTH;

EID: 84886291802     PISSN: 15524868     EISSN: 15524876     Source Type: Journal    
DOI: 10.1002/ajmg.c.31382     Document Type: Article

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