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Results 1 - 10 of 45 for Hypertrophic cardiomyopathy 7
  1. ... Registry: Hypertrophic cardiomyopathy 4 Genetic Testing Registry: Hypertrophic cardiomyopathy 7 Familial hypertrophic cardiomyopathy National Organization for Rare Disorders ( ...
  2. ... PubMed Berko BA, Swift M. X-linked dilated cardiomyopathy. N Engl J Med. 1987 May 7;316(19):1186-91. doi: 10.1056/NEJM198705073161904. Citation on PubMed Cohen N, Muntoni F. Multiple pathogenetic mechanisms in X linked dilated cardiomyopathy. Heart. 2004 Aug;90(8):835-41. doi: ...
  3. ... Morales A, Hershberger RE. Genetic evaluation of dilated cardiomyopathy. Curr Cardiol Rep. 2013 Jul;15(7):375. doi: 10.1007/s11886-013-0375-1. Citation on PubMed Posafalvi A, Herkert JC, Sinke RJ, van den Berg MP, ... gene card for: dilated cardiomyopathy (CMD). Eur J Hum Genet. 2013 Oct;21( ...
  4. ... VENTRICULAR NONCOMPACTION 10; LVNC10 CARDIOMYOPATHY, DILATED, 1R; CMD1R CARDIOMYOPATHY, DILATED, 1S; CMD1S LEFT VENTRICULAR NONCOMPACTION 7; LVNC7 PubMed Bennett CE, Freudenberger R. The Current ...
  5. ... and its deficiency causes centronuclear myopathy with dilated cardiomyopathy. Am J Hum Genet. 2014 Aug 7;95(2):218-26. doi: 10.1016/j. ...
  6. ... mutation of mitochondrial DNAJC19 causing dilated and noncompaction cardiomyopathy, anemia, ataxia, and male genital anomalies. Pediatr Res. 2012 Oct;72(4):432-7. doi: 10.1038/pr.2012.92. Epub 2012 ...
  7. ... PubMed Muchtar E, Blauwet LA, Gertz MA. Restrictive Cardiomyopathy: Genetics, Pathogenesis, Clinical Manifestations, Diagnosis, and Therapy. Circ Res. 2017 Sep 15;121(7):819-837. doi: 10.1161/CIRCRESAHA.117.310982. ...
  8. ... L, Mandel H, Wevers RA. Autosomal recessive dilated cardiomyopathy due to DOLK mutations results from abnormal dystroglycan O-mannosylation. PLoS Genet. 2011 Dec;7(12):e1002427. doi: 10.1371/journal.pgen.1002427. ...
  9. ... right, arrhythmogenic ... 7 Genetic Testing Registry: Arrhythmogenic right ventricular dysplasia 1 ...
  10. ... 10.1038/nrendo.2010.210. Epub 2010 Dec 7. Citation on PubMed Hoffman JD, Jacobson Z, Young TL, Marshall JD, Kaplan P. Familial variable expression of dilated cardiomyopathy in Alstrom syndrome: a report of four sibs. ...
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