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| pubmed-article:17940600 | lifeskim:mentions | umls-concept:C0015320 | lld:lifeskim |
| pubmed-article:17940600 | lifeskim:mentions | umls-concept:C0025663 | lld:lifeskim |
| pubmed-article:17940600 | lifeskim:mentions | umls-concept:C1511726 | lld:lifeskim |
| pubmed-article:17940600 | lifeskim:mentions | umls-concept:C0008630 | lld:lifeskim |
| pubmed-article:17940600 | lifeskim:mentions | umls-concept:C0439064 | lld:lifeskim |
| pubmed-article:17940600 | lifeskim:mentions | umls-concept:C0205352 | lld:lifeskim |
| pubmed-article:17940600 | lifeskim:mentions | umls-concept:C2828360 | lld:lifeskim |
| pubmed-article:17940600 | pubmed:issue | 10 | lld:pubmed |
| pubmed-article:17940600 | pubmed:dateCreated | 2007-10-17 | lld:pubmed |
| pubmed-article:17940600 | pubmed:abstractText | Over the past decade many linkage studies have defined chromosomal intervals containing polymorphisms that modulate a variety of traits. Many phenotypes are now associated with enough mapping data that meta-analysis could help refine locations of known QTLs and detect many novel QTLs. | lld:pubmed |
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| pubmed-article:17940600 | pubmed:language | eng | lld:pubmed |
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| pubmed-article:17940600 | pubmed:citationSubset | IM | lld:pubmed |
| pubmed-article:17940600 | pubmed:status | MEDLINE | lld:pubmed |
| pubmed-article:17940600 | pubmed:issn | 1932-6203 | lld:pubmed |
| pubmed-article:17940600 | pubmed:author | pubmed-author:XXX | lld:pubmed |
| pubmed-article:17940600 | pubmed:author | pubmed-author:WilliamsRober... | lld:pubmed |
| pubmed-article:17940600 | pubmed:author | pubmed-author:BromanKarl... | lld:pubmed |
| pubmed-article:17940600 | pubmed:author | pubmed-author:PeirceJeremy... | lld:pubmed |
| pubmed-article:17940600 | pubmed:issnType | Electronic | lld:pubmed |
| pubmed-article:17940600 | pubmed:volume | 2 | lld:pubmed |
| pubmed-article:17940600 | pubmed:owner | NLM | lld:pubmed |
| pubmed-article:17940600 | pubmed:authorsComplete | Y | lld:pubmed |
| pubmed-article:17940600 | pubmed:pagination | e1036 | lld:pubmed |
| pubmed-article:17940600 | pubmed:dateRevised | 2010-11-18 | lld:pubmed |
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| pubmed-article:17940600 | pubmed:year | 2007 | lld:pubmed |
| pubmed-article:17940600 | pubmed:articleTitle | A simple method for combining genetic mapping data from multiple crosses and experimental designs. | lld:pubmed |
| pubmed-article:17940600 | pubmed:affiliation | Center for Neuroscience, Department of Anatomy and Neurobiology, University of Tennessee Health Science Center, Memphis, Tennessee, United States of America. jpeirce@utmem.edu | lld:pubmed |
| pubmed-article:17940600 | pubmed:publicationType | Journal Article | lld:pubmed |
| pubmed-article:17940600 | pubmed:publicationType | Research Support, U.S. Gov't, Non-P.H.S. | lld:pubmed |
| pubmed-article:17940600 | pubmed:publicationType | Research Support, N.I.H., Extramural | lld:pubmed |
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