Statements in which the resource exists as a subject.
PredicateObject
rdf:type
lifeskim:mentions
pubmed:issue
10
pubmed:dateCreated
2010-10-25
pubmed:abstractText
To investigate the relationship of WNT8b and SHH genes mutation and Hirschsprung disease(HSCR) in Chinese children.
pubmed:language
chi
pubmed:journal
pubmed:citationSubset
IM
pubmed:chemical
pubmed:status
MEDLINE
pubmed:month
Oct
pubmed:issn
1671-0274
pubmed:author
pubmed:issnType
Print
pubmed:volume
13
pubmed:owner
NLM
pubmed:authorsComplete
Y
pubmed:pagination
758-61
pubmed:meshHeading
pubmed:year
2010
pubmed:articleTitle
[Mutation and expression of WNT8b gene and SHH gene in Hirschsprung disease].
pubmed:affiliation
Key Laboratory of Congenital Malformation Reseach, The Ministry of Health, Shengjing Affiliated Hospital, China Medical University, Shenyang 110004, China. gaohong515@sina.com
pubmed:publicationType
Journal Article, English Abstract, Research Support, Non-U.S. Gov't