Isolated oligodontia associated with mutations in EDARADD, AXIN2, MSX1, and PAX9 genes

American Journal of Medical Genetics, Part A

Volumn 155, Issue 7, 2011, Pages 1616-1622

  Bergendal, Birgitta ^a   Klar, Joakim ^b   Stecksén Blicks, Christina ^c   Norderyd, Johanna ^a   Dahl, Niklas ^b  

^a INSTITUTE FOR POSTGRADUATE DENTAL EDUCATION   (Sweden)

^b UPPSALA UNIVERSITY   (Sweden)

^c UMEÅ UNIVERSITY   (Sweden)

Author keywords

Ectodermal dysplasia; EDARADD; Isolated oligodontia; Mutation screening

Indexed keywords

GENOMIC DNA;

ARTICLE; AXIN2 GENE; COHORT ANALYSIS; CONTROLLED STUDY; DENATURING GRADIENT GEL ELECTROPHORESIS; DNA SEQUENCE; ECTODERM; EDA GENE; EDAR GENE; EDARADD GENE; FAMILY HISTORY; FEMALE; GENE MUTATION; GENETIC ASSOCIATION; GENETIC CODE; HUMAN; HUMAN TISSUE; MAJOR CLINICAL STUDY; MALE; MSX1 GENE; MUTATIONAL ANALYSIS; OLIGODONTIA; PAX9 GENE; PREVALENCE; PRIORITY JOURNAL; SELF REPORT; SWEDEN;

ANODONTIA; CYTOSKELETAL PROTEINS; EDAR-ASSOCIATED DEATH DOMAIN PROTEIN; FEMALE; GENETIC ASSOCIATION STUDIES; GENETIC PREDISPOSITION TO DISEASE; HUMANS; MALE; MSX1 TRANSCRIPTION FACTOR; MUTATION; PAX9 TRANSCRIPTION FACTOR;

EID: 79959505447     PISSN: 15524825     EISSN: 15524833     Source Type: Journal    
DOI: 10.1002/ajmg.a.34045     Document Type: Article

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