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Table representation of search results timeline featuring number of search results per year.
Year | Number of Results |
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2006 | 1 |
2013 | 1 |
2014 | 2 |
2016 | 1 |
2017 | 1 |
2024 | 0 |
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Page 1
Genetics of hypertrophic cardiomyopathy in Norway.
Clin Genet. 2014 Oct;86(4):355-60. doi: 10.1111/cge.12286. Epub 2013 Oct 23.
Clin Genet. 2014.
PMID: 24111713
Single-gene mutations and increased left ventricular wall thickness in the community: the Framingham Heart Study.
Morita H, Larson MG, Barr SC, Vasan RS, O'Donnell CJ, Hirschhorn JN, Levy D, Corey D, Seidman CE, Seidman JG, Benjamin EJ.
Morita H, et al.
Circulation. 2006 Jun 13;113(23):2697-705. doi: 10.1161/CIRCULATIONAHA.105.593558. Epub 2006 Jun 5.
Circulation. 2006.
PMID: 16754800
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Malignant effects of multiple rare variants in sarcomere genes on the prognosis of patients with hypertrophic cardiomyopathy.
Wang J, Wang Y, Zou Y, Sun K, Wang Z, Ding H, Yuan J, Wei W, Hou Q, Wang H, Liu X, Zhang H, Ji Y, Zhou X, Sharma RK, Wang D, Ahmad F, Hui R, Song L.
Wang J, et al.
Eur J Heart Fail. 2014 Sep;16(9):950-7. doi: 10.1002/ejhf.144. Epub 2014 Jul 31.
Eur J Heart Fail. 2014.
PMID: 25132132
Free article.
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Reassessment of Mendelian gene pathogenicity using 7,855 cardiomyopathy cases and 60,706 reference samples.
Walsh R, Thomson KL, Ware JS, Funke BH, Woodley J, McGuire KJ, Mazzarotto F, Blair E, Seller A, Taylor JC, Minikel EV, Exome Aggregation Consortium, MacArthur DG, Farrall M, Cook SA, Watkins H.
Walsh R, et al.
Genet Med. 2017 Feb;19(2):192-203. doi: 10.1038/gim.2016.90. Epub 2016 Aug 17.
Genet Med. 2017.
PMID: 27532257
Free PMC article.
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