WNT10A mutations also associated with agenesis of the maxillary permanent canines, a separate entity

American Journal of Medical Genetics, Part A

Volumn 164, Issue 2, 2014, Pages 360-363

  Kantaputra, P ^a,b   Kaewgahya, M ^a   Kantaputra, W ^a,b  

^a CHIANG MAI UNIVERSITY   (Thailand)

^b Dentaland Clinic   (Thailand)

Author keywords

Dens invaginatus; Ectodermal dysplasia; Hypodontia; Hypotrichosis; Microdontia; Missing teeth; Nail dysplasia; Odonto onycho dermal dysplasia; Peg shaped lateral incisor; Sparse hair; Tricho odonto onycho dermal dysplasia

Indexed keywords

WNT10A PROTEIN;

AMINO ACID SUBSTITUTION; ARTICLE; AUTOSOMAL DOMINANT INHERITANCE; CANINE TOOTH; CLINICAL ARTICLE; CONTROLLED STUDY; FEMALE; GENE IDENTIFICATION; GENETIC ASSOCIATION; HETEROZYGOSITY; HUMAN; HYPODONTIA; MALE; MISSENSE MUTATION; MOUTH EXAMINATION; MUTATIONAL ANALYSIS; PRIORITY JOURNAL; WNT10A GENE;

DENS INVAGINATUS; ECTODERMAL DYSPLASIA; HYPODONTIA; HYPOTRICHOSIS; MICRODONTIA; MISSING TEETH; NAIL DYSPLASIA; ODONTO-ONYCHO-DERMAL DYSPLASIA; PEG-SHAPED LATERAL INCISOR; SPARSE HAIR; TRICHO-ODONTO-ONYCHO-DERMAL DYSPLASIA;

ANODONTIA; DNA MUTATIONAL ANALYSIS; FEMALE; HETEROZYGOTE; HUMANS; MALE; MAXILLA; MUTATION; WNT PROTEINS;

EID: 84892900838     PISSN: 15524825     EISSN: 15524833     Source Type: Journal    
DOI: 10.1002/ajmg.a.36280     Document Type: Article

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