Interferon regulatory factor 6 (IRF6) and fibroblast growth factor receptor 1 (FGFR1) contribute to human tooth agenesis

American Journal of Medical Genetics, Part A

Volumn 143, Issue 6, 2007, Pages 538-545

  Vieira, Alexandre R ^a   Modesto, Adriana ^a,b   Meira, Raquel ^c   Barbosa, Anna Renata Schneider ^b   Lidral, Andrew C ^d,e   Murray, Jeffrey C ^f  

^a UNIVERSITY OF PITTSBURGH   (United States)

^b FEDERAL UNIVERSITY OF RIO DE JANEIRO   (Brazil)

^c UNIVERSIDADE LUTERANA DO BRASIL   (Brazil)

^d UNIVERSITY OF IOWA   (United States)

^e UNIVERSITY OF IOWA   (United States)

^f UNIVERSITY OF IOWA   (United States)

Author keywords

Cleft lip and palate; Hypodontia; Kallmann syndrome; MSX1; Muscle segment; Oligodontia; Orofacial clefts; Paired box; PAX9; TGFA; Transforming growth factor alpha; Van der Woude syndrome

Indexed keywords

ADOLESCENT; ADULT; ALLELE; ARTICLE; CHILD; CLEFT LIP PALATE; DISEASE ASSOCIATION; DNA DETERMINATION; FEMALE; FGFR1 GENE; GENE; GENE INTERACTION; GENE LINKAGE DISEQUILIBRIUM; GENE MUTATION; GENETIC ANALYSIS; GENETIC ASSOCIATION; GENETIC MARKER; GENOTYPE PHENOTYPE CORRELATION; HUMAN; HYPODONTIA; IRF6 GENE; MAJOR CLINICAL STUDY; MALE; MOLAR TOOTH; MSX1 GENE; POLYMERASE CHAIN REACTION; PRIORITY JOURNAL; RECEPTOR GENE; REGULATOR GENE; TGFA GENE; VAN DER WOUDE SYNDROME; WEBBED NECK;

ADOLESCENT; ADULT; ALGORITHMS; ALLELES; ANODONTIA; CHILD; FAMILY HEALTH; FEMALE; GENE FREQUENCY; GENETIC MARKERS; GENETIC PREDISPOSITION TO DISEASE; GENOTYPE; HAPLOTYPES; HUMANS; INTERFERON REGULATORY FACTORS; LINKAGE DISEQUILIBRIUM; MALE; MIDDLE AGED; MSX1 TRANSCRIPTION FACTOR; POLYMORPHISM, SINGLE NUCLEOTIDE; RECEPTOR, FIBROBLAST GROWTH FACTOR, TYPE 1; TRANSFORMING GROWTH FACTOR ALPHA;

EID: 33847368959     PISSN: 15524825     EISSN: 15524833     Source Type: Journal    
DOI: 10.1002/ajmg.a.31620     Document Type: Article

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