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rdf:type |
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lifeskim:mentions |
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pubmed:issue |
5
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pubmed:dateCreated |
2011-4-28
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pubmed:abstractText |
Congenital diaphragmatic hernia (CDH) is a life threatening birth defect. Most of the genetic factors that contribute to the development of CDH remain unidentified.
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pubmed:grant |
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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 |
May
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pubmed:issn |
1468-6244
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pubmed:author |
pubmed-author:CheungSau WaiSW,
pubmed-author:DanhaiveOlivierO,
pubmed-author:FernandesCaraciolo JCJ,
pubmed-author:HanchardNeilN,
pubmed-author:HogueJacobJ,
pubmed-author:HolderAshley MAM,
pubmed-author:JohnsonAnthonyA,
pubmed-author:LallyKevin PKP,
pubmed-author:RauenKatherine AKA,
pubmed-author:SchaibleThomasT,
pubmed-author:ScottDaryl ADA,
pubmed-author:ShchelochkovOleg AOA,
pubmed-author:SlavotinekAnneA,
pubmed-author:TibboelDickD,
pubmed-author:TonkVijay SVS,
pubmed-author:VeenmaDanielleD,
pubmed-author:WatJeanette JJJ,
pubmed-author:WatMargaret JMJ,
pubmed-author:YuZhiyinZ,
pubmed-author:de KleinAnneliesA
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pubmed:issnType |
Electronic
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pubmed:volume |
48
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pubmed:owner |
NLM
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pubmed:authorsComplete |
Y
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pubmed:pagination |
299-307
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pubmed:meshHeading |
pubmed-meshheading:21525063-Amino Acid Substitution,
pubmed-meshheading:21525063-Child, Preschool,
pubmed-meshheading:21525063-Chromosome Aberrations,
pubmed-meshheading:21525063-Chromosomes, Human, Pair 1,
pubmed-meshheading:21525063-Chromosomes, Human, Pair 11,
pubmed-meshheading:21525063-Chromosomes, Human, Pair 16,
pubmed-meshheading:21525063-Chromosomes, Human, Pair 17,
pubmed-meshheading:21525063-Chromosomes, Human, Pair 8,
pubmed-meshheading:21525063-Comparative Genomic Hybridization,
pubmed-meshheading:21525063-DNA-Binding Proteins,
pubmed-meshheading:21525063-Diaphragmatic Eventration,
pubmed-meshheading:21525063-Female,
pubmed-meshheading:21525063-Genome, Human,
pubmed-meshheading:21525063-Hernia, Diaphragmatic,
pubmed-meshheading:21525063-Humans,
pubmed-meshheading:21525063-Infant,
pubmed-meshheading:21525063-Infant, Newborn,
pubmed-meshheading:21525063-Male,
pubmed-meshheading:21525063-Mutation,
pubmed-meshheading:21525063-Transcription Factors
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pubmed:year |
2011
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pubmed:articleTitle |
Genomic alterations that contribute to the development of isolated and non-isolated congenital diaphragmatic hernia.
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pubmed:affiliation |
Department of Molecular and Human Genetics, Baylor College of Medicine, Houston, Texas 77030, USA.
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pubmed:publicationType |
Journal Article,
Research Support, Non-U.S. Gov't,
Research Support, N.I.H., Extramural
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