| pubmed-article:8358441 | rdf:type | pubmed:Citation | lld:pubmed |
| pubmed-article:8358441 | lifeskim:mentions | umls-concept:C0949658 | lld:lifeskim |
| pubmed-article:8358441 | lifeskim:mentions | umls-concept:C0017337 | lld:lifeskim |
| pubmed-article:8358441 | lifeskim:mentions | umls-concept:C0008653 | lld:lifeskim |
| pubmed-article:8358441 | lifeskim:mentions | umls-concept:C0679622 | lld:lifeskim |
| pubmed-article:8358441 | lifeskim:mentions | umls-concept:C1283195 | lld:lifeskim |
| pubmed-article:8358441 | lifeskim:mentions | umls-concept:C0205314 | lld:lifeskim |
| pubmed-article:8358441 | pubmed:issue | 3 | lld:pubmed |
| pubmed-article:8358441 | pubmed:dateCreated | 1993-9-24 | lld:pubmed |
| pubmed-article:8358441 | pubmed:abstractText | Familial hypertrophic cardiomyopathy (FHC) is a cardiac disorder transmitted as an autosomal dominant trait. FHC has been shown to be genetically heterogeneous with less than 50% of published pedigrees being associated with mutations in the beta myosin heavy chain (beta-MHC) gene on chromosome 14q11-q12. A second locus has recently been reported on chromosome 1. We examined the segregation of microsatellite markers in a French pedigree for which the disease is not linked to beta-MHC gene. We found significant linkage of the disease locus to several (CA)n repeats located on chromosome 11 (lod scores between +3.3 and +4.98). The data suggest the localization of the novel FHC gene in a region spanning 17 centiMorgans. | lld:pubmed |
| pubmed-article:8358441 | pubmed:language | eng | lld:pubmed |
| pubmed-article:8358441 | pubmed:journal | http://linkedlifedata.com/r... | lld:pubmed |
| pubmed-article:8358441 | pubmed:citationSubset | IM | lld:pubmed |
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| pubmed-article:8358441 | pubmed:status | MEDLINE | lld:pubmed |
| pubmed-article:8358441 | pubmed:month | Jul | lld:pubmed |
| pubmed-article:8358441 | pubmed:issn | 1061-4036 | lld:pubmed |
| pubmed-article:8358441 | pubmed:author | pubmed-author:BeckmannJ SJS | lld:pubmed |
| pubmed-article:8358441 | pubmed:author | pubmed-author:GuicheneyPP | lld:pubmed |
| pubmed-article:8358441 | pubmed:author | pubmed-author:DufourCC | lld:pubmed |
| pubmed-article:8358441 | pubmed:author | pubmed-author:BercoviciJJ | lld:pubmed |
| pubmed-article:8358441 | pubmed:author | pubmed-author:WisnewskyCC | lld:pubmed |
| pubmed-article:8358441 | pubmed:author | pubmed-author:CarrierLL | lld:pubmed |
| pubmed-article:8358441 | pubmed:author | pubmed-author:DausseEE | lld:pubmed |
| pubmed-article:8358441 | pubmed:author | pubmed-author:HengstenbergC... | lld:pubmed |
| pubmed-article:8358441 | pubmed:author | pubmed-author:Berebbi-Bertr... | lld:pubmed |
| pubmed-article:8358441 | pubmed:author | pubmed-author:PulvenisDD | lld:pubmed |
| pubmed-article:8358441 | pubmed:issnType | Print | lld:pubmed |
| pubmed-article:8358441 | pubmed:volume | 4 | lld:pubmed |
| pubmed-article:8358441 | pubmed:geneSymbol | FHC | lld:pubmed |
| pubmed-article:8358441 | pubmed:owner | NLM | lld:pubmed |
| pubmed-article:8358441 | pubmed:authorsComplete | N | lld:pubmed |
| pubmed-article:8358441 | pubmed:pagination | 311-3 | lld:pubmed |
| pubmed-article:8358441 | pubmed:dateRevised | 2010-11-18 | lld:pubmed |
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| pubmed-article:8358441 | pubmed:year | 1993 | lld:pubmed |
| pubmed-article:8358441 | pubmed:articleTitle | Mapping of a novel gene for familial hypertrophic cardiomyopathy to chromosome 11. | lld:pubmed |
| pubmed-article:8358441 | pubmed:affiliation | INSERM U127, Hôpital Lariboisière, Paris, France. | lld:pubmed |
| pubmed-article:8358441 | pubmed:publicationType | Journal Article | lld:pubmed |
| pubmed-article:8358441 | pubmed:publicationType | Research Support, Non-U.S. Gov't | lld:pubmed |
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