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rdf:type |
|
|
lifeskim:mentions |
|
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pubmed:issue |
22
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pubmed:dateCreated |
2006-7-20
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pubmed:abstractText |
To investigate the distribution of the single nucleotide polymorphism (SNP) sites in TBX1 gene and the distribution of related haplotypes in the patients with conotruncal defects (CTD) and normal people.
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pubmed:language |
chi
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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 |
Jun
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pubmed:issn |
0376-2491
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pubmed:author |
|
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pubmed:issnType |
Print
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pubmed:day |
13
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pubmed:volume |
86
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pubmed:owner |
NLM
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pubmed:authorsComplete |
Y
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pubmed:pagination |
1553-7
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pubmed:meshHeading |
pubmed-meshheading:16854283-Adolescent,
pubmed-meshheading:16854283-Adult,
pubmed-meshheading:16854283-Case-Control Studies,
pubmed-meshheading:16854283-Child,
pubmed-meshheading:16854283-Child, Preschool,
pubmed-meshheading:16854283-Haploidy,
pubmed-meshheading:16854283-Heart Defects, Congenital,
pubmed-meshheading:16854283-Humans,
pubmed-meshheading:16854283-Infant,
pubmed-meshheading:16854283-Polymorphism, Single Nucleotide,
pubmed-meshheading:16854283-T-Box Domain Proteins
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pubmed:year |
2006
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|
pubmed:articleTitle |
[Single nucleotide polymorphism and haplotype in TBX1 gene of patients with conotruncal defects: analysis of 130 cases].
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|
pubmed:affiliation |
Department of Cardiology, Second Affiliated Hospital of China Medical University, Shenyang 110004, China.
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pubmed:publicationType |
Journal Article,
English Abstract
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