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2. Clinical and genetical heterogeneity of familial hypertrophic cardiomyopathy. Hengstenberg C; Carrier L; Schwartz K; Maisch B Herz; 1994 Apr; 19(2):84-90. PubMed ID: 8194836 [TBL] [Abstract][Full Text] [Related]
3. Familial hypertrophic cardiomyopathy. Microsatellite haplotyping and identification of a hot spot for mutations in the beta-myosin heavy chain gene. Dausse E; Komajda M; Fetler L; Dubourg O; Dufour C; Carrier L; Wisnewsky C; Bercovici J; Hengstenberg C; al-Mahdawi S J Clin Invest; 1993 Dec; 92(6):2807-13. PubMed ID: 8254035 [TBL] [Abstract][Full Text] [Related]
4. Mutations in cardiac myosin heavy chain genes cause familial hypertrophic cardiomyopathy. Seidman CE; Seidman JG Mol Biol Med; 1991 Apr; 8(2):159-66. PubMed ID: 1806760 [TBL] [Abstract][Full Text] [Related]
5. Myosin mutations in hypertrophic cardiomyopathy and functional implications. Vosberg HP Herz; 1994 Apr; 19(2):75-83. PubMed ID: 8194835 [TBL] [Abstract][Full Text] [Related]
6. Preclinical diagnosis of familial hypertrophic cardiomyopathy by genetic analysis of blood lymphocytes. Rosenzweig A; Watkins H; Hwang DS; Miri M; McKenna W; Traill TA; Seidman JG; Seidman CE N Engl J Med; 1991 Dec; 325(25):1753-60. PubMed ID: 1944483 [TBL] [Abstract][Full Text] [Related]
7. Molecular genetics of cardiomyopathies. Marian AJ; Roberts R Herz; 1993 Aug; 18(4):230-7. PubMed ID: 8375803 [TBL] [Abstract][Full Text] [Related]
8. Characteristics and prognostic implications of myosin missense mutations in familial hypertrophic cardiomyopathy. Watkins H; Rosenzweig A; Hwang DS; Levi T; McKenna W; Seidman CE; Seidman JG N Engl J Med; 1992 Apr; 326(17):1108-14. PubMed ID: 1552912 [TBL] [Abstract][Full Text] [Related]
9. Identification of a mutation near a functional site of the beta cardiac myosin heavy chain gene in a family with hypertrophic cardiomyopathy. Dufour C; Dausse E; Fetler L; Dubourg O; Bouhour JB; Vosberg HP; Guicheney P; Komajda M; Schwartz K J Mol Cell Cardiol; 1994 Sep; 26(9):1241-7. PubMed ID: 7815466 [TBL] [Abstract][Full Text] [Related]
10. Skeletal muscle expression and abnormal function of beta-myosin in hypertrophic cardiomyopathy. Cuda G; Fananapazir L; Zhu WS; Sellers JR; Epstein ND J Clin Invest; 1993 Jun; 91(6):2861-5. PubMed ID: 8514894 [TBL] [Abstract][Full Text] [Related]
11. Double heterozygosity for mutations in the beta-myosin heavy chain and in the cardiac myosin binding protein C genes in a family with hypertrophic cardiomyopathy. Richard P; Isnard R; Carrier L; Dubourg O; Donatien Y; Mathieu B; Bonne G; Gary F; Charron P; Hagege M; Komajda M; Schwartz K; Hainque B J Med Genet; 1999 Jul; 36(7):542-5. PubMed ID: 10424815 [TBL] [Abstract][Full Text] [Related]
12. Mapping of a novel gene for familial hypertrophic cardiomyopathy to chromosome 11. Carrier L; Hengstenberg C; Beckmann JS; Guicheney P; Dufour C; Bercovici J; Dausse E; Berebbi-Bertrand I; Wisnewsky C; Pulvenis D Nat Genet; 1993 Jul; 4(3):311-3. PubMed ID: 8358441 [TBL] [Abstract][Full Text] [Related]
13. [Hypertrophic cardiomyopathy: practical application of genetic research]. Guicheney P; Schwartz K; Komajda M Arch Mal Coeur Vaiss; 1995 Apr; 88(4 Suppl):569-71. PubMed ID: 7487301 [TBL] [Abstract][Full Text] [Related]
14. Missense mutation of the beta-cardiac myosin heavy-chain gene in hypertrophic cardiomyopathy. Arai S; Matsuoka R; Hirayama K; Sakurai H; Tamura M; Ozawa T; Kimura M; Imamura S; Furutani Y; Joh-o K Am J Med Genet; 1995 Sep; 58(3):267-76. PubMed ID: 8533830 [TBL] [Abstract][Full Text] [Related]
15. Molecular basis of hypertrophic and dilated cardiomyopathy. Marian AJ; Roberts R Tex Heart Inst J; 1994; 21(1):6-15. PubMed ID: 8180512 [TBL] [Abstract][Full Text] [Related]
16. [Cardiomyopathies from the aspect of molecular cardiology]. Kölbel F Cas Lek Cesk; 1994 Jun; 133(13):401-3. PubMed ID: 8062332 [TBL] [Abstract][Full Text] [Related]
17. Characterization of mutant myosins of Dictyostelium discoideum equivalent to human familial hypertrophic cardiomyopathy mutants. Molecular force level of mutant myosins may have a prognostic implication. Fujita H; Sugiura S; Momomura S; Omata M; Sugi H; Sutoh K J Clin Invest; 1997 Mar; 99(5):1010-5. PubMed ID: 9062359 [TBL] [Abstract][Full Text] [Related]
18. [Familial hypertrophic cardiomyopathy: genes, mutations and animal models. A review]. Ramírez CD; Padrón R Invest Clin; 2004 Mar; 45(1):69-99. PubMed ID: 15058760 [TBL] [Abstract][Full Text] [Related]
19. Novel locus for an inherited cardiomyopathy maps to chromosome 7. Song L; DePalma SR; Kharlap M; Zenovich AG; Cirino A; Mitchell R; McDonough B; Maron BJ; Seidman CE; Seidman JG; Ho CY Circulation; 2006 May; 113(18):2186-92. PubMed ID: 16651466 [TBL] [Abstract][Full Text] [Related]
20. One third of Danish hypertrophic cardiomyopathy patients with MYH7 mutations have mutations [corrected] in MYH7 rod region. Hougs L; Havndrup O; Bundgaard H; Køber L; Vuust J; Larsen LA; Christiansen M; Andersen PS Eur J Hum Genet; 2005 Feb; 13(2):161-5. PubMed ID: 15483641 [TBL] [Abstract][Full Text] [Related] [Next] [New Search]