Statements in which the resource exists as a subject.
PredicateObject
rdf:type
lifeskim:mentions
pubmed:issue
9
pubmed:dateCreated
2010-9-27
pubmed:abstractText
Orofacial clefts are among the most common birth defects with a strong genetic component. Nonsyndromic cleft palate (NSCP) is a complex malformation determined by the interaction between multiple genes and environmental risk factors.
pubmed:language
eng
pubmed:journal
pubmed:citationSubset
IM
pubmed:chemical
pubmed:status
MEDLINE
pubmed:month
Sep
pubmed:issn
1542-0760
pubmed:author
pubmed:copyrightInfo
© 2010 Wiley-Liss, Inc.
pubmed:issnType
Electronic
pubmed:volume
88
pubmed:owner
NLM
pubmed:authorsComplete
Y
pubmed:pagination
748-56
pubmed:meshHeading
pubmed-meshheading:20672350-Baltic States, pubmed-meshheading:20672350-Case-Control Studies, pubmed-meshheading:20672350-Cleft Lip, pubmed-meshheading:20672350-Cleft Palate, pubmed-meshheading:20672350-Collagen Type II, pubmed-meshheading:20672350-Collagen Type XI, pubmed-meshheading:20672350-Epistasis, Genetic, pubmed-meshheading:20672350-Female, pubmed-meshheading:20672350-Gene Expression Regulation, Developmental, pubmed-meshheading:20672350-Genetic Association Studies, pubmed-meshheading:20672350-Genetic Markers, pubmed-meshheading:20672350-Genetic Predisposition to Disease, pubmed-meshheading:20672350-Haplotypes, pubmed-meshheading:20672350-Humans, pubmed-meshheading:20672350-Interferon Regulatory Factors, pubmed-meshheading:20672350-Male, pubmed-meshheading:20672350-Polymorphism, Single Nucleotide, pubmed-meshheading:20672350-Risk Factors, pubmed-meshheading:20672350-Signal Transduction
pubmed:year
2010
pubmed:articleTitle
Genetic variants in COL2A1, COL11A2, and IRF6 contribute risk to nonsyndromic cleft palate.
pubmed:affiliation
Institute of Molecular and Cell Biology, University of Tartu, Tartu, Estonia. tiitn@ebc.ee
pubmed:publicationType
Journal Article, Research Support, Non-U.S. Gov't