Statements in which the resource exists as a subject.
PredicateObject
rdf:type
lifeskim:mentions
pubmed:issue
6
pubmed:dateCreated
2008-12-9
pubmed:abstractText
To investigate the association of Axis inhibitor-2 (AXIN2) gene rs2240308, rs8081536 and rs9913621 single nucleotide polymorphisms (SNPs) with Hirschsprung disease(HSCR).
pubmed:language
chi
pubmed:journal
pubmed:citationSubset
IM
pubmed:chemical
pubmed:status
MEDLINE
pubmed:month
Dec
pubmed:issn
1003-9406
pubmed:author
pubmed:issnType
Print
pubmed:volume
25
pubmed:owner
NLM
pubmed:authorsComplete
Y
pubmed:pagination
697-700
pubmed:dateRevised
2011-11-17
pubmed:meshHeading
pubmed-meshheading:19065536-Adolescent, pubmed-meshheading:19065536-Axin Protein, pubmed-meshheading:19065536-Base Sequence, pubmed-meshheading:19065536-Case-Control Studies, pubmed-meshheading:19065536-Child, pubmed-meshheading:19065536-Child, Preschool, pubmed-meshheading:19065536-Cytoskeletal Proteins, pubmed-meshheading:19065536-DNA Mutational Analysis, pubmed-meshheading:19065536-Exons, pubmed-meshheading:19065536-Female, pubmed-meshheading:19065536-Gene Frequency, pubmed-meshheading:19065536-Genetic Predisposition to Disease, pubmed-meshheading:19065536-Genotype, pubmed-meshheading:19065536-Hirschsprung Disease, pubmed-meshheading:19065536-Humans, pubmed-meshheading:19065536-Infant, pubmed-meshheading:19065536-Male, pubmed-meshheading:19065536-Polymerase Chain Reaction, pubmed-meshheading:19065536-Polymorphism, Single Nucleotide
pubmed:year
2008
pubmed:articleTitle
[Association of single nucleotide polymorphisms of Axis inhibitor-2 gene rs224030, rs8081536, rs9913621 with Hirschsprung disease].
pubmed:affiliation
Key Laboratory of Congenital Malformation Research, Ministry of Health, Shengjing Affiliated Hospital, China Medical University, Shenyang, Liaoning 110004, P. R. China. gaohong515@sina.com
pubmed:publicationType
Journal Article, English Abstract