Mutations in wnt10a are present in more than half of isolated hypodontia cases

Journal of Medical Genetics

Volumn 49, Issue 5, 2012, Pages 327-331

  van den Boogaard, Marie José ^a   Créton, Marijn ^a   Bronkhorst, Yvon ^a   van der Hout, Annemieke ^b   Hennekam, Eric ^a   Lindhout, Dick ^a   Cune, Marco ^b,c   van Amstel, Hans Kristian Ploos ^a  

^a UNIVERSITY MEDICAL CENTER UTRECHT   (Netherlands)

^b UNIVERSITY MEDICAL CENTER GRONINGEN   (Netherlands)

^c ST ANTONIUS HOSPITAL   (Netherlands)

Author keywords

[No Author keywords available]

Indexed keywords

ADOLESCENT; ADULT; AGENESIS; ARTICLE; AXIN2 GENE; CHILD; CLINICAL ARTICLE; FEMALE; GENE; GENE MUTATION; GENOTYPE; HUMAN; HYPODONTIA; IRF6 GENE; MALE; MSX1 GENE; NUCLEOTIDE SEQUENCE; PAX9 GENE; PHENOTYPE; PRESCHOOL CHILD; PRIORITY JOURNAL; SCHOOL CHILD; SEQUENCE ANALYSIS; WNT10A GENE;

ADOLESCENT; ADULT; ANODONTIA; AXIN PROTEIN; CHILD; DNA MUTATIONAL ANALYSIS; FEMALE; HUMANS; MALE; MIDDLE AGED; MSX1 TRANSCRIPTION FACTOR; MUTATION; PAX9 TRANSCRIPTION FACTOR; PHENOTYPE; WNT PROTEINS;

EID: 84864094899     PISSN: 00222593     EISSN: 14686244     Source Type: Journal    
DOI: 10.1136/jmedgenet-2012-100750     Document Type: Article

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