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Mortality Risk Associated With Truncating Founder Mutations in Titin.
Circ Genom Precis Med. 2019 May;12(5):e002436. doi: 10.1161/CIRCGEN.118.002436.
Circ Genom Precis Med. 2019.
PMID: 31112426
Functional assessment of potential splice site variants in arrhythmogenic right ventricular dysplasia/cardiomyopathy.
Groeneweg JA, Ummels A, Mulder M, Bikker H, van der Smagt JJ, van Mil AM, Homfray T, Post JG, Elvan A, van der Heijden JF, Houweling AC, Jongbloed JD, Wilde AA, van Tintelen JP, Hauer RN, Dooijes D.
Groeneweg JA, et al.
Heart Rhythm. 2014 Nov;11(11):2010-7. doi: 10.1016/j.hrthm.2014.07.041. Epub 2014 Jul 31.
Heart Rhythm. 2014.
PMID: 25087486
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Clinical and genetic characterization of patients with arrhythmogenic right ventricular dysplasia/cardiomyopathy caused by a plakophilin-2 splice mutation.
van der Smagt JJ, van der Zwaag PA, van Tintelen JP, Cox MG, Wilde AA, van Langen IM, Ummels A, Hennekam FA, Dooijes D, Gerbens F, Bikker H, Hauer RN, Doevendans PA.
van der Smagt JJ, et al.
Cardiology. 2012;123(3):181-9. doi: 10.1159/000342717. Epub 2012 Nov 7.
Cardiology. 2012.
PMID: 23147395
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Multiple Small Supernumerary Marker Chromosomes Resulting from Maternal Meiosis I or II Errors.
Hochstenbach R, Nowakowska B, Volleth M, Ummels A, Kutkowska-Kaźmierczak A, Obersztyn E, Ziemkiewicz K, Gerloff C, Schanze D, Zenker M, Muschke P, Schanze I, Poot M, Liehr T.
Hochstenbach R, et al.
Mol Syndromol. 2016 Feb;6(5):210-21. doi: 10.1159/000441408. Epub 2015 Oct 31.
Mol Syndromol. 2016.
PMID: 26997941
Free PMC article.
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