Phenotypic variation in FAM83H-associated amelogenesis imperfecta

Journal of Dental Research

Volumn 88, Issue 4, 2009, Pages 356-360

  Wright, J T ^a   Frazier Bowers, S ^b   Simmons, D ^a   Alexander, K ^b   Crawford, P ^c   Han, S T ^d   Hart, P S ^e   Hart, T C ^d  

^a UNIVERSITY OF NORTH CAROLINA   (United States)

^b UNIVERSITY OF NORTH CAROLINA   (United States)

^c UNIVERSITY OF BRISTOL   (United Kingdom)

^d NATIONAL INSTITUTE OF DENTAL AND CRANIOFACIAL RESEARCH   (United States)

^e NATIONAL HUMAN GENOME RESEARCH INSTITUTE   (United States)

Author keywords

Amelogenesis imperfecta; Craniofacial; Enamel; FAM83H; Hypocalcified; Phenotype

Indexed keywords

ENAMEL PROTEIN; FAM83H PROTEIN, HUMAN; PROTEIN;

AMELOGENESIS IMPERFECTA; ARTICLE; CEPHALOMETRY; CRANIOFACIAL MALFORMATION; GENE DELETION; GENETICS; HUMAN; MAXILLOFACIAL DEVELOPMENT; METABOLISM; NUCLEOTIDE SEQUENCE; PEDIGREE; STOP CODON;

AMELOGENESIS IMPERFECTA; BASE SEQUENCE; CEPHALOMETRY; CODON, NONSENSE; CRANIOFACIAL ABNORMALITIES; DENTAL ENAMEL PROTEINS; HUMANS; MAXILLOFACIAL DEVELOPMENT; PEDIGREE; PROTEINS; SEQUENCE DELETION;

EID: 66149136519     PISSN: 00220345     EISSN: None     Source Type: Journal    
DOI: 10.1177/0022034509333822     Document Type: Article

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