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Table representation of search results timeline featuring number of search results per year.
Year | Number of Results |
---|---|
2014 | 1 |
2015 | 1 |
2016 | 1 |
2017 | 2 |
2019 | 1 |
2020 | 1 |
2024 | 0 |
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Page 1
Novel genotype-phenotype associations demonstrated by high-throughput sequencing in patients with hypertrophic cardiomyopathy.
Heart. 2015 Feb;101(4):294-301. doi: 10.1136/heartjnl-2014-306387. Epub 2014 Oct 28.
Heart. 2015.
PMID: 25351510
Free PMC article.
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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Burden of Recurrent and Ancestral Mutations in Families With Hypertrophic Cardiomyopathy.
Ross SB, Bagnall RD, Ingles J, Van Tintelen JP, Semsarian C.
Ross SB, et al.
Circ Cardiovasc Genet. 2017 Jun;10(3):e001671. doi: 10.1161/CIRCGENETICS.116.001671.
Circ Cardiovasc Genet. 2017.
PMID: 28615295
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Thin filament dysfunctions caused by mutations in tropomyosin Tpm3.12 and Tpm1.1.
Moraczewska J.
Moraczewska J.
J Muscle Res Cell Motil. 2020 Mar;41(1):39-53. doi: 10.1007/s10974-019-09532-y. Epub 2019 Jul 3.
J Muscle Res Cell Motil. 2020.
PMID: 31270709
Free PMC article.
Review.
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