Statements in which the resource exists as a subject.
PredicateObject
rdf:type
lifeskim:mentions
pubmed:issue
1
pubmed:dateCreated
2008-2-5
pubmed:abstractText
To investigate the point mutations and polymorphisms of SIP1 gene in Hirschsprung disease(HSCR) and discuss the relationship between the feature of gene mutations and single nucleotide polymorphisms of SIP1 gene and HSCR.
pubmed:language
chi
pubmed:journal
pubmed:citationSubset
IM
pubmed:chemical
pubmed:status
MEDLINE
pubmed:month
Feb
pubmed:issn
1003-9406
pubmed:author
pubmed:issnType
Print
pubmed:volume
25
pubmed:owner
NLM
pubmed:authorsComplete
Y
pubmed:pagination
82-5
pubmed:dateRevised
2011-9-28
pubmed:meshHeading
pubmed:year
2008
pubmed:articleTitle
[Coding-sequence point mutation and polymorphism analyses of SIP1 gene in Hirschsprung disease].
pubmed:affiliation
Shengjing Affiliated Hospital, China Medical University, Shenyang, Liaoning, 110004 People's Republic of China.
pubmed:publicationType
Journal Article, English Abstract, Research Support, Non-U.S. Gov't