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L Thierfelder

Showing results (21-30 of 31) with videos related to

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Nature Genetics|April 1, 1993
A disease locus for familial hypertrophic cardiomyopathy maps to chromosome 1q3H Watkins, C MacRae, L Thierfelder, et al.
Cell|June 3, 1994
Alpha-tropomyosin and cardiac troponin T mutations cause familial hypertrophic cardiomyopathy: a disease of the sarcomereL Thierfelder, H Watkins, C MacRae, et al.
Genomics|January 16, 1999
Fine-structure mapping of the hereditary inclusion body myopathy locusI Eisenberg, C Thiel, T Levi, et al.
Circulation|January 1, 1994
An evaluation of ribonuclease protection assays for the detection of beta-cardiac myosin heavy chain gene mutationsC A MacRae, H C Watkins, J A Jarcho, et al.
Proceedings of the National Academy of Sciences of the United States of America|July 1, 1993
A familial hypertrophic cardiomyopathy locus maps to chromosome 15q2L Thierfelder, C MacRae, H Watkins, et al.
The Journal of Clinical Investigation|January 1, 1994
Prognostic implications of novel beta cardiac myosin heavy chain gene mutations that cause familial hypertrophic cardiomyopathyR Anan, G Greve, L Thierfelder, et al.
Nature Genetics|December 1, 1995
Mutations in the cardiac myosin binding protein-C gene on chromosome 11 cause familial hypertrophic cardiomyopathyH Watkins, D Conner, L Thierfelder, et al.
Biochemistry|April 15, 1997
Effects of two familial hypertrophic cardiomyopathy-causing mutations on alpha-tropomyosin structure and functionN Golitsina, Y An, N J Greenfield, et al.
The New England Journal of Medicine|April 20, 1995
Mutations in the genes for cardiac troponin T and alpha-tropomyosin in hypertrophic cardiomyopathyH Watkins, W J McKenna, L Thierfelder, et al.
Journal of the American College of Cardiology|March 1, 1997
Clinical features of hypertrophic cardiomyopathy caused by mutation of a "hot spot" in the alpha-tropomyosin geneD A Coviello, B J Maron, P Spirito, et al.
Pageof 4

Showing results (21-30 of 31) with videos related to

Sort By:
Pageof 4
Nature Genetics|April 1, 1993
A disease locus for familial hypertrophic cardiomyopathy maps to chromosome 1q3H Watkins, C MacRae, L Thierfelder, et al.
Cell|June 3, 1994
Alpha-tropomyosin and cardiac troponin T mutations cause familial hypertrophic cardiomyopathy: a disease of the sarcomereL Thierfelder, H Watkins, C MacRae, et al.
Genomics|January 16, 1999
Fine-structure mapping of the hereditary inclusion body myopathy locusI Eisenberg, C Thiel, T Levi, et al.
Circulation|January 1, 1994
An evaluation of ribonuclease protection assays for the detection of beta-cardiac myosin heavy chain gene mutationsC A MacRae, H C Watkins, J A Jarcho, et al.
Proceedings of the National Academy of Sciences of the United States of America|July 1, 1993
A familial hypertrophic cardiomyopathy locus maps to chromosome 15q2L Thierfelder, C MacRae, H Watkins, et al.
The Journal of Clinical Investigation|January 1, 1994
Prognostic implications of novel beta cardiac myosin heavy chain gene mutations that cause familial hypertrophic cardiomyopathyR Anan, G Greve, L Thierfelder, et al.
Nature Genetics|December 1, 1995
Mutations in the cardiac myosin binding protein-C gene on chromosome 11 cause familial hypertrophic cardiomyopathyH Watkins, D Conner, L Thierfelder, et al.
Biochemistry|April 15, 1997
Effects of two familial hypertrophic cardiomyopathy-causing mutations on alpha-tropomyosin structure and functionN Golitsina, Y An, N J Greenfield, et al.
The New England Journal of Medicine|April 20, 1995
Mutations in the genes for cardiac troponin T and alpha-tropomyosin in hypertrophic cardiomyopathyH Watkins, W J McKenna, L Thierfelder, et al.
Journal of the American College of Cardiology|March 1, 1997
Clinical features of hypertrophic cardiomyopathy caused by mutation of a "hot spot" in the alpha-tropomyosin geneD A Coviello, B J Maron, P Spirito, et al.
Pageof 4