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Year | Number of Results |
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2013 | 1 |
2014 | 1 |
2015 | 1 |
2021 | 1 |
2024 | 0 |
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The landscape of genetic variation in dilated cardiomyopathy as surveyed by clinical DNA sequencing.
Genet Med. 2014 Aug;16(8):601-8. doi: 10.1038/gim.2013.204. Epub 2014 Feb 6.
Genet Med. 2014.
PMID: 24503780
Free article.
Whole-exome sequencing in undiagnosed genetic diseases: interpreting 119 trios.
Zhu X, Petrovski S, Xie P, Ruzzo EK, Lu YF, McSweeney KM, Ben-Zeev B, Nissenkorn A, Anikster Y, Oz-Levi D, Dhindsa RS, Hitomi Y, Schoch K, Spillmann RC, Heimer G, Marek-Yagel D, Tzadok M, Han Y, Worley G, Goldstein J, Jiang YH, Lancet D, Pras E, Shashi V, McHale D, Need AC, Goldstein DB.
Zhu X, et al.
Genet Med. 2015 Oct;17(10):774-81. doi: 10.1038/gim.2014.191. Epub 2015 Jan 15.
Genet Med. 2015.
PMID: 25590979
Free PMC article.
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Genetic and Phenotypic Landscape of Peripartum Cardiomyopathy.
Goli R, Li J, Brandimarto J, Levine LD, Riis V, McAfee Q, DePalma S, Haghighi A, Seidman JG, Seidman CE, Jacoby D, Macones G, Judge DP, Rana S, Margulies KB, Cappola TP, Alharethi R, Damp J, Hsich E, Elkayam U, Sheppard R, Alexis JD, Boehmer J, Kamiya C, Gustafsson F, Damm P, Ersbøll AS, Goland S, Hilfiker-Kleiner D, McNamara DM; IMAC-2 and IPAC Investigators; Arany Z.
Goli R, et al.
Circulation. 2021 May 11;143(19):1852-1862. doi: 10.1161/CIRCULATIONAHA.120.052395. Epub 2021 Apr 20.
Circulation. 2021.
PMID: 33874732
Free PMC article.
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Compound heterozygosity of predicted loss-of-function DES variants in a family with recessive desminopathy.
McLaughlin HM, Kelly MA, Hawley PP, Darras BT, Funke B, Picker J.
McLaughlin HM, et al.
BMC Med Genet. 2013 Jul 2;14:68. doi: 10.1186/1471-2350-14-68.
BMC Med Genet. 2013.
PMID: 23815709
Free PMC article.
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