|
rdf:type |
|
|
lifeskim:mentions |
|
|
pubmed:issue |
9
|
|
pubmed:dateCreated |
2005-9-9
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|
pubmed:abstractText |
Patients with zinc finger homeo box 1B (ZFHX1B) mutations or deletions develop multiple congenital anomalies including Hirschsprung disease, known as Mowat-Wilson syndrome (MWS). In this study, we investigated variations in the enteric neural plexus abnormalities in MWS using morphometry-based histopathologic analysis.
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pubmed:language |
eng
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|
pubmed:journal |
|
|
pubmed:citationSubset |
IM
|
|
pubmed:chemical |
|
|
pubmed:status |
MEDLINE
|
|
pubmed:month |
Sep
|
|
pubmed:issn |
1531-5037
|
|
pubmed:author |
|
|
pubmed:issnType |
Electronic
|
|
pubmed:volume |
40
|
|
pubmed:owner |
NLM
|
|
pubmed:authorsComplete |
Y
|
|
pubmed:pagination |
1411-9
|
|
pubmed:dateRevised |
2007-5-30
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|
pubmed:meshHeading |
pubmed-meshheading:16150342-Anthropometry,
pubmed-meshheading:16150342-Child, Preschool,
pubmed-meshheading:16150342-Colon, Sigmoid,
pubmed-meshheading:16150342-Female,
pubmed-meshheading:16150342-Hirschsprung Disease,
pubmed-meshheading:16150342-Homeodomain Proteins,
pubmed-meshheading:16150342-Humans,
pubmed-meshheading:16150342-Male,
pubmed-meshheading:16150342-Mutation,
pubmed-meshheading:16150342-Rectum,
pubmed-meshheading:16150342-Repressor Proteins
|
|
pubmed:year |
2005
|
|
pubmed:articleTitle |
Variations in aganglionic segment length of the enteric neural plexus in Mowat-Wilson syndrome.
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|
pubmed:affiliation |
Department of Pediatrics, Nagoya University Graduate School of Medicine, Nagoya, Aichi 466-8550, Japan.
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|
pubmed:publicationType |
Journal Article,
Case Reports,
Research Support, Non-U.S. Gov't
|
