Novel MSX1 mutation in a family with autosomal-dominant hypodontia of second premolars and third molars

Archives of Oral Biology

Volumn 57, Issue 6, 2012, Pages 790-795

  Mostowska, Adrianna ^a   Biedziak, Barbara ^a,b   Jagodzinski, Pawel P ^a  

^a POZNAN UNIVERSITY OF MEDICAL SCIENCES   (Poland)

^b Private Dental Clinic   (Poland)

Author keywords

Hypodontia; MSX1; Mutation; PAX9; Second premolars

Indexed keywords

MSX1 PROTEIN, HUMAN; PAX9 PROTEIN, HUMAN; TRANSCRIPTION FACTOR MSX1; TRANSCRIPTION FACTOR PAX9;

ADOLESCENT; ARTICLE; CASE CONTROL STUDY; CONGENITAL MALFORMATION; DOMINANT GENE; FEMALE; GENETICS; HUMAN; HYPODONTIA; MOLAR TOOTH; MUTATION; NUCLEOTIDE SEQUENCE; PEDIGREE; PREMOLAR TOOTH;

ADOLESCENT; ANODONTIA; BICUSPID; CASE-CONTROL STUDIES; DNA MUTATIONAL ANALYSIS; FEMALE; GENES, DOMINANT; HUMANS; MOLAR, THIRD; MSX1 TRANSCRIPTION FACTOR; MUTATION; PAX9 TRANSCRIPTION FACTOR; PEDIGREE;

EID: 84861622484     PISSN: 00039969     EISSN: None     Source Type: Journal    
DOI: 10.1016/j.archoralbio.2012.01.003     Document Type: Article

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