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Results 1 - 10 of 108 for Hypertrophic cardiomyopathy 12
  1. Familial hypertrophic cardiomyopathy 
    ... HYPERTROPHIC, 25; CMH25 CARDIOMYOPATHY, FAMILIAL HYPERTROPHIC, 11; CMH11 CARDIOMYOPATHY, FAMILIAL HYPERTROPHIC, 12; CMH12 CARDIOMYOPATHY, FAMILIAL HYPERTROPHIC, 7; CMH7 CARDIOMYOPATHY, FAMILIAL ...
    https://medlineplus.gov/.../familial-hypertrophic-cardiomyopathy - Genetics
  2. RAF1 gene 
    ... mutations cause Noonan and LEOPARD syndromes with hypertrophic cardiomyopathy. Nat Genet. 2007 Aug;39(8):1007-12. doi: 10.1038/ng2073. Epub 2007 Jul 1. ...
    https://medlineplus.gov/genetics/gene/raf1 - Genetics
  3. Familial dilated cardiomyopathy 
    ... Siegfried JD. Clinical and genetic issues in dilated cardiomyopathy: a review for genetics professionals. Genet Med. 2010 Nov;12(11):655-67. doi: 10.1097/GIM.0b013e3181f2481f. ...
    https://medlineplus.gov/.../familial-dilated-cardiomyopathy - Genetics
  4. MYBPC3 gene 
    ... in the molecular genetics of left ventricular noncompaction cardiomyopathy. Clin Chim Acta. 2017 Feb;465:40-44. doi: 10.1016/j.cca.2016.12.013. Epub 2016 Dec 15. Citation on PubMed ...
    https://medlineplus.gov/genetics/gene/mybpc3 - Genetics
  5. Left ventricular noncompaction 
    ... in the molecular genetics of left ventricular noncompaction cardiomyopathy. Clin Chim Acta. 2017 Feb;465:40-44. doi: 10.1016/j.cca.2016.12.013. Epub 2016 Dec 15. Citation on PubMed ...
    https://medlineplus.gov/.../condition/left-ventricular-noncompaction - Genetics
  6. MYH7 gene 
    ... in the molecular genetics of left ventricular noncompaction cardiomyopathy. Clin Chim Acta. 2017 Feb;465:40-44. doi: 10.1016/j.cca.2016.12.013. Epub 2016 Dec 15. Citation on PubMed ...
    https://medlineplus.gov/genetics/gene/myh7 - Genetics
  7. PKP2 gene 
    ... the molecular phenotype of two arrhythmogenic right ventricular cardiomyopathy (ARVC)-related plakophilin-2 (PKP2) mutations. Heart Rhythm. 2008 Dec;5(12):1715-23. doi: 10.1016/j.hrthm.2008. ...
    https://medlineplus.gov/genetics/gene/pkp2 - Genetics
  8. ALG12-congenital disorder of glycosylation 
    ... Ig): sibs with a unique skeletal dysplasia, hypogammaglobulinemia, cardiomyopathy, genital malformations, and early lethality. Am J Med Genet A. 2007 Jun 15;143A(12):1371-8. doi: 10.1002/ajmg.a.31791. ...
    https://medlineplus.gov/...lg12-congenital-disorder-of-glycosylation - Genetics
  9. DOLK-congenital disorder of glycosylation 
    ... 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. Epub ...
    https://medlineplus.gov/...dolk-congenital-disorder-of-glycosylation - Genetics
  10. POMT1 gene 
    ... Bertini E, Angelini C, Tosatto SC, Pegoraro E. Cardiomyopathy in patients with POMT1-related congenital and limb-girdle muscular dystrophy. Eur J Hum Genet. 2012 Dec;20(12):1234-9. doi: 10.1038/ejhg.2012.71. ...
    https://medlineplus.gov/genetics/gene/pomt1 - Genetics
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