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rdf:type |
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lifeskim:mentions |
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pubmed:issue |
1
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pubmed:dateCreated |
2010-2-3
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pubmed:abstractText |
Mutations in the receptor tyrosine kinase RET gene are associated with Hirschsprung disease (HD), which is also known as congenital intestinal aganglionosis. We found an association with specific alleles in five single nucleotide polymorphism (SNP) sites of the RET gene in our HD patients.
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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 |
Jan
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pubmed:issn |
0929-6646
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pubmed:author |
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pubmed:issnType |
Print
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pubmed:volume |
109
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pubmed:owner |
NLM
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pubmed:authorsComplete |
Y
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pubmed:pagination |
32-8
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pubmed:meshHeading |
pubmed-meshheading:20123584-Alleles,
pubmed-meshheading:20123584-DNA,
pubmed-meshheading:20123584-Digestive System Abnormalities,
pubmed-meshheading:20123584-Exons,
pubmed-meshheading:20123584-Genetic Predisposition to Disease,
pubmed-meshheading:20123584-Genotype,
pubmed-meshheading:20123584-Hirschsprung Disease,
pubmed-meshheading:20123584-Hospitals, University,
pubmed-meshheading:20123584-Humans,
pubmed-meshheading:20123584-Immunohistochemistry,
pubmed-meshheading:20123584-Intestinal Pseudo-Obstruction,
pubmed-meshheading:20123584-Polymerase Chain Reaction,
pubmed-meshheading:20123584-Polymorphism, Single Nucleotide,
pubmed-meshheading:20123584-Proto-Oncogene Proteins c-ret,
pubmed-meshheading:20123584-Sequence Analysis, DNA,
pubmed-meshheading:20123584-Taiwan
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pubmed:year |
2010
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pubmed:articleTitle |
Polymorphisms of the RET gene in hirschsprung disease, anorectal malformation and intestinal pseudo-obstruction in Taiwan.
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pubmed:affiliation |
Department of Pediatric Surgery, Chung Shan Medical University Hospital, Taichung, Taiwan.
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pubmed:publicationType |
Journal Article,
Comparative Study,
Research Support, Non-U.S. Gov't
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