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3. Genotype phenotype correlations of cardiac beta-myosin heavy chain mutations in Indian patients with hypertrophic and dilated cardiomyopathy. Rai TS; Ahmad S; Bahl A; Ahuja M; Ahluwalia TS; Singh B; Talwar KK; Khullar M Mol Cell Biochem; 2009 Jan; 321(1-2):189-96. PubMed ID: 18953637 [TBL] [Abstract][Full Text] [Related]
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5. [Mutation analysis of beta myosin heavy chain gene in hypertrophic cardiomyopathy families]. Fan XP; Yang ZW; Feng XL; Yang FH; Xiao B; Liang Y Zhonghua Yi Xue Yi Chuan Xue Za Zhi; 2011 Aug; 28(4):387-92. PubMed ID: 21811976 [TBL] [Abstract][Full Text] [Related]
6. Genotype-phenotype analysis in four families with mutations in beta-myosin heavy chain gene responsible for familial hypertrophic cardiomyopathy. Tesson F; Richard P; Charron P; Mathieu B; Cruaud C; Carrier L; Dubourg O; Lautié N; Desnos M; Millaire A; Isnard R; Hagege AA; Bouhour JB; Bennaceur M; Hainque B; Guicheney P; Schwartz K; Komajda M Hum Mutat; 1998; 12(6):385-92. PubMed ID: 9829907 [TBL] [Abstract][Full Text] [Related]
7. An ARG403GLN beta-myosin heavy chain gene mutation identified in an Italian family with hypertrophic cardiomyopathy; description of clinical features of the family members. Conte MR; Morelio M; Mangiardi L; Orzan F; Checco L; Bonfiglio G; Alfarano A; Camaschella C; Brusca A Eur Heart J; 1997 Jun; 18(6):1033-4. PubMed ID: 9183600 [No Abstract] [Full Text] [Related]
8. Homozygotes for a R869G mutation in the beta -myosin heavy chain gene have a severe form of familial hypertrophic cardiomyopathy. Richard P; Charron P; Leclercq C; Ledeuil C; Carrier L; Dubourg O; Desnos M; Bouhour JB; Schwartz K; Daubert JC; Komajda M; Hainque B J Mol Cell Cardiol; 2000 Aug; 32(8):1575-83. PubMed ID: 10900182 [TBL] [Abstract][Full Text] [Related]
10. Prognostic significance of beta-myosin heavy chain mutations is reflective of their hypertrophic expressivity in patients with hypertrophic cardiomyopathy. Abchee A; Marian AJ J Investig Med; 1997 Apr; 45(4):191-6. PubMed ID: 9154300 [TBL] [Abstract][Full Text] [Related]
11. Development and application of linkage analysis in genetic diagnosis of familial hypertrophic cardiomyopathy. Mogensen J; Andersen PS; Steffensen U; Christiansen M; Egeblad H; Gregersen N; Børglum AD J Med Genet; 2001 Mar; 38(3):193-8. PubMed ID: 11303515 [No Abstract] [Full Text] [Related]
19. Novel association of hypertrophic cardiomyopathy, sensorineural deafness, and a mutation in unconventional myosin VI (MYO6). Mohiddin SA; Ahmed ZM; Griffith AJ; Tripodi D; Friedman TB; Fananapazir L; Morell RJ J Med Genet; 2004 Apr; 41(4):309-14. PubMed ID: 15060111 [No Abstract] [Full Text] [Related]
20. Expression of HCM causing mutations: lessons learnt from genotype-phenotype studies of the South African founder MYH7 A797T mutation. Moolman-Smook J; De Lange W; Corfield V; Brink P J Med Genet; 2000 Dec; 37(12):951-6. PubMed ID: 11186938 [No Abstract] [Full Text] [Related] [Next] [New Search]