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Year | Number of Results |
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2013 | 1 |
2014 | 2 |
2016 | 1 |
2017 | 2 |
2024 | 0 |
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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
A case of an infant with compound heterozygous mutations for hypertrophic cardiomyopathy producing a phenotype of left ventricular noncompaction.
Haberer K, Buffo-Sequeira I, Chudley AE, Spriggs E, Sergi C.
Haberer K, et al.
Can J Cardiol. 2014 Oct;30(10):1249.e1-3. doi: 10.1016/j.cjca.2014.05.021. Epub 2014 Jun 12.
Can J Cardiol. 2014.
PMID: 25262865
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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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Nonfamilial Hypertrophic Cardiomyopathy: Prevalence, Natural History, and Clinical Implications.
Ingles J, Burns C, Bagnall RD, Lam L, Yeates L, Sarina T, Puranik R, Briffa T, Atherton JJ, Driscoll T, Semsarian C.
Ingles J, et al.
Circ Cardiovasc Genet. 2017 Apr;10(2):e001620. doi: 10.1161/CIRCGENETICS.116.001620.
Circ Cardiovasc Genet. 2017.
PMID: 28408708
Free article.
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