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rdf:type |
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lifeskim:mentions |
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pubmed:dateCreated |
2007-7-20
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pubmed:abstractText |
Copy number polymorphisms caused by genomic rearrangements like deletions, make a significant contribution to the genomic differences between two individuals and may add to disease predisposition. Therefore, genotyping of such deletion polymorphisms in case-control studies could give important insights into risk associations.
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pubmed:commentsCorrections |
http://linkedlifedata.com/resource/pubmed/commentcorrection/17598925-11702203,
http://linkedlifedata.com/resource/pubmed/commentcorrection/17598925-11823792,
http://linkedlifedata.com/resource/pubmed/commentcorrection/17598925-12151349,
http://linkedlifedata.com/resource/pubmed/commentcorrection/17598925-12533830,
http://linkedlifedata.com/resource/pubmed/commentcorrection/17598925-12574941,
http://linkedlifedata.com/resource/pubmed/commentcorrection/17598925-14557987,
http://linkedlifedata.com/resource/pubmed/commentcorrection/17598925-15273396,
http://linkedlifedata.com/resource/pubmed/commentcorrection/17598925-15286789,
http://linkedlifedata.com/resource/pubmed/commentcorrection/17598925-15313892,
http://linkedlifedata.com/resource/pubmed/commentcorrection/17598925-15895083,
http://linkedlifedata.com/resource/pubmed/commentcorrection/17598925-15918152,
http://linkedlifedata.com/resource/pubmed/commentcorrection/17598925-16255080,
http://linkedlifedata.com/resource/pubmed/commentcorrection/17598925-16327808,
http://linkedlifedata.com/resource/pubmed/commentcorrection/17598925-16327809,
http://linkedlifedata.com/resource/pubmed/commentcorrection/17598925-16418744,
http://linkedlifedata.com/resource/pubmed/commentcorrection/17598925-16468122,
http://linkedlifedata.com/resource/pubmed/commentcorrection/17598925-16497726,
http://linkedlifedata.com/resource/pubmed/commentcorrection/17598925-16606630,
http://linkedlifedata.com/resource/pubmed/commentcorrection/17598925-16651370,
http://linkedlifedata.com/resource/pubmed/commentcorrection/17598925-16826518,
http://linkedlifedata.com/resource/pubmed/commentcorrection/17598925-16838144,
http://linkedlifedata.com/resource/pubmed/commentcorrection/17598925-17122850,
http://linkedlifedata.com/resource/pubmed/commentcorrection/17598925-8650574,
http://linkedlifedata.com/resource/pubmed/commentcorrection/17598925-9875838
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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:issn |
1471-2156
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pubmed:author |
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pubmed:issnType |
Electronic
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pubmed:volume |
8
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pubmed:owner |
NLM
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pubmed:authorsComplete |
Y
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pubmed:pagination |
41
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pubmed:dateRevised |
2010-11-18
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pubmed:meshHeading |
pubmed-meshheading:17598925-Adolescent,
pubmed-meshheading:17598925-Adult,
pubmed-meshheading:17598925-Aged,
pubmed-meshheading:17598925-Aged, 80 and over,
pubmed-meshheading:17598925-Breast Neoplasms,
pubmed-meshheading:17598925-Case-Control Studies,
pubmed-meshheading:17598925-DNA Primers,
pubmed-meshheading:17598925-Female,
pubmed-meshheading:17598925-Gene Deletion,
pubmed-meshheading:17598925-Genotype,
pubmed-meshheading:17598925-Homozygote,
pubmed-meshheading:17598925-Humans,
pubmed-meshheading:17598925-Middle Aged,
pubmed-meshheading:17598925-Polymerase Chain Reaction,
pubmed-meshheading:17598925-Polymorphism, Single Nucleotide,
pubmed-meshheading:17598925-Risk Factors,
pubmed-meshheading:17598925-Sequence Alignment,
pubmed-meshheading:17598925-Trypsin,
pubmed-meshheading:17598925-Trypsinogen
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pubmed:year |
2007
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pubmed:articleTitle |
High-throughput genotyping of a common deletion polymorphism disrupting the TRY6 gene and its association with breast cancer risk.
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pubmed:affiliation |
Division of Molecular Genetic Epidemiology, German Cancer Research Center (DKFZ), Im Neuenheimer Feld 580, Heidelberg, Germany. wagner_ke@yahoo.de <wagner_ke@yahoo.de>
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pubmed:publicationType |
Journal Article,
Research Support, Non-U.S. Gov't
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