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rdf:type |
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lifeskim:mentions |
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pubmed:issue |
5
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pubmed:dateCreated |
2005-10-10
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pubmed:abstractText |
In the candidate region 12q13 of simple congenital heart disease(CHD), four single nucleotide polymorphisms(SNPs) in HOXC4 gene were chosen in order to investigate the distribution of SNP and haplotypes in simple CHD patients and normal people.
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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 |
Oct
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pubmed:issn |
1003-9406
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pubmed:author |
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pubmed:issnType |
Print
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pubmed:volume |
22
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pubmed:owner |
NLM
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pubmed:authorsComplete |
Y
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pubmed:pagination |
497-501
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pubmed:meshHeading |
pubmed-meshheading:16215934-Adolescent,
pubmed-meshheading:16215934-Adult,
pubmed-meshheading:16215934-Alleles,
pubmed-meshheading:16215934-Base Sequence,
pubmed-meshheading:16215934-Child,
pubmed-meshheading:16215934-Chromosomes, Human, Pair 12,
pubmed-meshheading:16215934-DNA Mutational Analysis,
pubmed-meshheading:16215934-Gene Frequency,
pubmed-meshheading:16215934-Genetic Predisposition to Disease,
pubmed-meshheading:16215934-Genotype,
pubmed-meshheading:16215934-Haplotypes,
pubmed-meshheading:16215934-Heart Defects, Congenital,
pubmed-meshheading:16215934-Homeodomain Proteins,
pubmed-meshheading:16215934-Humans,
pubmed-meshheading:16215934-Middle Aged,
pubmed-meshheading:16215934-Molecular Sequence Data,
pubmed-meshheading:16215934-Polymorphism, Single Nucleotide,
pubmed-meshheading:16215934-Young Adult
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pubmed:year |
2005
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pubmed:articleTitle |
Analysis of single nucleotide polymorphisms and haplotypes in HOXC gene cluster within susceptible region 12q13 of simple congenital heart disease.
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pubmed:affiliation |
Department of Medical Genetics, China Medical University, Shenyang, Liaoning, PR China.
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pubmed:publicationType |
Journal Article,
Research Support, Non-U.S. Gov't
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