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rdf:type |
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lifeskim:mentions |
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pubmed:issue |
8
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pubmed:dateCreated |
2002-7-31
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pubmed:abstractText |
The aim of this report is to describe the pattern of similarities among the patients, exemplifying a newly recognized form of Hirschsprung's disease (HSCR) caused by mutations of ZFHX1B encoding Smad interacting protein-1.
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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 |
Aug
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pubmed:issn |
1531-5037
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pubmed:author |
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pubmed:copyrightInfo |
Copyright 2002, Elsevier Science (USA). All rights reserved.
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pubmed:issnType |
Electronic
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pubmed:volume |
37
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pubmed:owner |
NLM
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pubmed:authorsComplete |
Y
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pubmed:pagination |
1117-22
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pubmed:dateRevised |
2007-5-30
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pubmed:meshHeading |
pubmed-meshheading:12149685-Adult,
pubmed-meshheading:12149685-Child,
pubmed-meshheading:12149685-Chromosome Mapping,
pubmed-meshheading:12149685-Chromosomes, Human, Pair 13,
pubmed-meshheading:12149685-Chromosomes, Human, Pair 2,
pubmed-meshheading:12149685-Codon, Nonsense,
pubmed-meshheading:12149685-DNA-Binding Proteins,
pubmed-meshheading:12149685-Female,
pubmed-meshheading:12149685-Hirschsprung Disease,
pubmed-meshheading:12149685-Homeodomain Proteins,
pubmed-meshheading:12149685-Humans,
pubmed-meshheading:12149685-Infant, Newborn,
pubmed-meshheading:12149685-Male,
pubmed-meshheading:12149685-Repressor Proteins,
pubmed-meshheading:12149685-Retrospective Studies,
pubmed-meshheading:12149685-Sequence Deletion,
pubmed-meshheading:12149685-Smad Proteins,
pubmed-meshheading:12149685-Trans-Activators,
pubmed-meshheading:12149685-Translocation, Genetic
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pubmed:year |
2002
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pubmed:articleTitle |
Clinical features of a form of Hirschsprung's disease caused by a novel genetic abnormality.
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pubmed:affiliation |
Department of Pediatric Surgery, the Central Hospital, Aichi Prefectural Colony, Kasugai, Japan.
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pubmed:publicationType |
Journal Article,
Research Support, Non-U.S. Gov't
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