Genetic analysis of familial nonsyndromic primary failure of eruption

Orthodontics and Craniofacial Research

Volumn 12, Issue 2, 2009, Pages 74-81

  Frazier Bowers, S A ^a   Simmons, D ^b   Koehler, K ^c   Zhou, J ^a  

^a UNIVERSITY OF NORTH CAROLINA   (United States)

^b UNIVERSITY OF NORTH CAROLINA   (United States)

^c Private Practice   (United States)

Author keywords

Eruption failure; Linkage studies; Mutational analysis

Indexed keywords

AMBN PROTEIN, HUMAN; AMELOGENIN; AMELX PROTEIN, HUMAN; CELL ADHESION MOLECULE; ENAMEL PROTEIN; MICROSATELLITE DNA; POSTN PROTEIN, HUMAN; RUNX2 PROTEIN, HUMAN; TRANSCRIPTION FACTOR RUNX2;

ADOLESCENT; ADULT; AGED; ARTICLE; CHILD; CHROMOSOME 13; CHROMOSOME 15; CHROMOSOME 17; DOMINANT GENE; FEMALE; GENETIC LINKAGE; GENETIC MARKER; GENETIC POLYMORPHISM; GENETICS; GENOTYPE; HUMAN; INTRON; MALE; MIDDLE AGED; PEDIGREE; PENETRANCE; PHENOTYPE; PRESCHOOL CHILD; SINGLE NUCLEOTIDE POLYMORPHISM; TOOTH DISEASE; TOOTH ERUPTION;

ADOLESCENT; ADULT; AGED; AMELOGENIN; CELL ADHESION MOLECULES; CHILD; CHILD, PRESCHOOL; CHROMOSOMES, HUMAN, PAIR 13; CHROMOSOMES, HUMAN, PAIR 15; CHROMOSOMES, HUMAN, PAIR 17; CORE BINDING FACTOR ALPHA 1 SUBUNIT; DENTAL ENAMEL PROTEINS; FEMALE; GENES, DOMINANT; GENETIC MARKERS; GENOTYPE; HUMANS; INTRONS; LINKAGE (GENETICS); LOD SCORE; MALE; MICROSATELLITE REPEATS; MIDDLE AGED; PEDIGREE; PENETRANCE; PHENOTYPE; POLYMORPHISM, GENETIC; POLYMORPHISM, SINGLE NUCLEOTIDE; TOOTH DISEASES; TOOTH ERUPTION; YOUNG ADULT;

EID: 68049106152     PISSN: 16016335     EISSN: 16016343     Source Type: Journal    
DOI: 10.1111/j.1601-6343.2009.01440.x     Document Type: Article

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