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20972907
Source:
http://linkedlifedata.com/resource/pubmed/id/20972907
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pubmed-article:20972907
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pubmed-article:20972907
pubmed:issue
10
lld:pubmed
pubmed-article:20972907
pubmed:dateCreated
2010-10-25
lld:pubmed
pubmed-article:20972907
pubmed:abstractText
To investigate the relationship of WNT8b and SHH genes mutation and Hirschsprung disease(HSCR) in Chinese children.
lld:pubmed
pubmed-article:20972907
pubmed:language
chi
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pubmed-article:20972907
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http://linkedlifedata.com/r...
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IM
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MEDLINE
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pubmed:month
Oct
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pubmed-article:20972907
pubmed:issn
1671-0274
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pubmed-article:20972907
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pubmed-author:HuangYingY
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pubmed-author:GaoHongH
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Print
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13
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pubmed-article:20972907
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NLM
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pubmed:authorsComplete
Y
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pubmed-article:20972907
pubmed:year
2010
lld:pubmed
pubmed-article:20972907
pubmed:articleTitle
[Mutation and expression of WNT8b gene and SHH gene in Hirschsprung disease].
lld:pubmed
pubmed-article:20972907
pubmed:affiliation
Key Laboratory of Congenital Malformation Reseach, The Ministry of Health, Shengjing Affiliated Hospital, China Medical University, Shenyang 110004, China. gaohong515@sina.com
lld:pubmed
pubmed-article:20972907
pubmed:publicationType
Journal Article
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pubmed:publicationType
English Abstract
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pubmed-article:20972907
pubmed:publicationType
Research Support, Non-U.S. Gov't
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