RUNX2 mutations in cleidocranial dysplasia patients

Oral Diseases

Volumn 16, Issue 1, 2010, Pages 55-60

  Ryoo, H M ^a   Kang, H Y ^a   Lee, S K ^a   Lee, K E ^a   Kim, J W ^a,b  

^a School of Dentistry   (South Korea)

^b Seoul National University   (South Korea)

Author keywords

Cleidocranial dysplasia; Mutation; RUNX2; Supernumerary teeth

Indexed keywords

ARTICLE; CLEIDOCRANIAL DYSPLASIA; CRANIAL SUTURE; GENE MUTATION; HUMAN; MOLECULAR GENETICS; NONSENSE MUTATION; PHENOTYPE; PRIORITY JOURNAL; TOOTH DEVELOPMENT;

CHILD; CLEIDOCRANIAL DYSPLASIA; CODON, NONSENSE; CORE BINDING FACTOR ALPHA 1 SUBUNIT; DNA MUTATIONAL ANALYSIS; FEMALE; HUMANS; MALE; MUTATION, MISSENSE; PEDIGREE; POLYMORPHISM, SINGLE NUCLEOTIDE; TOOTH, SUPERNUMERARY;

EID: 73649122404     PISSN: 1354523X     EISSN: 16010825     Source Type: Journal    
DOI: 10.1111/j.1601-0825.2009.01623.x     Document Type: Article

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