rdf:type |
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lifeskim:mentions |
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pubmed:issue |
9
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pubmed:dateCreated |
2010-9-27
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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.
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pubmed:language |
eng
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pubmed:journal |
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pubmed:citationSubset |
IM
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pubmed:chemical |
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pubmed:status |
MEDLINE
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pubmed:month |
Sep
|
pubmed:issn |
1542-0760
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pubmed:author |
pubmed-author:AkotaIlzeI,
pubmed-author:AmbrozaityteLaimaL,
pubmed-author:BarkaneBirutaB,
pubmed-author:JagomägiTriinT,
pubmed-author:KrjutskovKaarelK,
pubmed-author:KruminaAstridaA,
pubmed-author:KucinskasVaidutisV,
pubmed-author:KucinskieneZita AusreleZA,
pubmed-author:LaceBaibaB,
pubmed-author:MatulevicieneAusraA,
pubmed-author:MetspaluAndresA,
pubmed-author:NikopensiusTiitT,
pubmed-author:PiekuseLindaL,
pubmed-author:PraneIngaI,
pubmed-author:SaagMareM,
pubmed-author:TammekiviVeronikaV
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pubmed:copyrightInfo |
© 2010 Wiley-Liss, Inc.
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pubmed:issnType |
Electronic
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pubmed:volume |
88
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pubmed:owner |
NLM
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pubmed:authorsComplete |
Y
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pubmed:pagination |
748-56
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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
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pubmed:year |
2010
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pubmed:articleTitle |
Genetic variants in COL2A1, COL11A2, and IRF6 contribute risk to nonsyndromic cleft palate.
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pubmed:affiliation |
Institute of Molecular and Cell Biology, University of Tartu, Tartu, Estonia. tiitn@ebc.ee
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pubmed:publicationType |
Journal Article,
Research Support, Non-U.S. Gov't
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