Polymorphisms in CHDH gene and the risk of tooth agenesis

Birth Defects Research Part A - Clinical and Molecular Teratology

Volumn 91, Issue 3, 2011, Pages 169-176

  Mostowska, Adrianna ^a   Biedziak, Barbara ^a   Dunin Wilczynska, Izabella ^b   Komorowska, Anna ^b   Jagodzinski, Pawel P ^a  

^a POZNAN UNIVERSITY OF MEDICAL SCIENCES   (Poland)

^b MEDICAL UNIVERSITY OF LUBLIN   (Poland)

Author keywords

CHDH; Folate and choline metabolism; Hypodontia; Oligodontia; PLD2

Indexed keywords

CHOLINE; FOLIC ACID;

ALLELE; ARTICLE; CONTROLLED STUDY; FEMALE; GENE IDENTIFICATION; GENE INTERACTION; GENETIC EPISTASIS; GENETIC POLYMORPHISM; GENETIC RISK; GENETIC SUSCEPTIBILITY; GENETIC VARIABILITY; HUMAN; HYPODONTIA; INTRON; MAJOR CLINICAL STUDY; MALE; POLAND; PRIORITY JOURNAL; SINGLE NUCLEOTIDE POLYMORPHISM;

CASE-CONTROL STUDIES; CHOLINE DEHYDROGENASE; DNA MUTATIONAL ANALYSIS; FEMALE; GENE FREQUENCY; GENETIC ASSOCIATION STUDIES; GENETIC PREDISPOSITION TO DISEASE; GENOTYPE; HUMANS; LINKAGE DISEQUILIBRIUM; MALE; MODELS, BIOLOGICAL; PHOSPHOLIPASE D; POLYMORPHISM, SINGLE NUCLEOTIDE; RISK FACTORS; TOOTH ABNORMALITIES;

EID: 79952589051     PISSN: 15420752     EISSN: 15420760     Source Type: Journal    
DOI: 10.1002/bdra.20771     Document Type: Article

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