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M F Leppert

Showing results (11-20 of 49) with videos related to

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Neurology|May 1, 1992
Evidence of genetic heterogeneity among the nondystrophic myotoniasL J Ptacek, F A Ziter, J W Roberts, et al.
Diabetes|May 20, 1999
A genome-wide search for type 2 diabetes susceptibility genes in Utah CaucasiansS C Elbein, M D Hoffman, K Teng, et al.
Journal of Hypertension|March 22, 2000
Evaluation of heterodimeric guanylyl cyclase genes as candidates for human hypertensionR S Danziger, C Pappas, C Barnitz, et al.
Neuromuscular Disorders : NMD|August 30, 2001
Genetic characterization of a large, historically significant Utah kindred with facioscapulohumeral dystrophyK M Flanigan, C M Coffeen, L Sexton, et al.
Diabetes|March 1, 1996
Linkage studies of NIDDM with 23 chromosome 11 markers in a sample of whites of northern European descentS C Elbein, K L Bragg, M D Hoffman, et al.
The European Respiratory Journal|December 24, 1998
Factor V Leiden is not common in patients diagnosed with primary pulmonary hypertensionC G Elliott, M F Leppert, G J Alexander, et al.
The Western Journal of Medicine|October 1, 1987
Mapping approaches to gene identification in humansR L White, J M Lalouel, G M Lathrop, et al.
American Journal of Human Genetics|August 1, 1996
Autosomal dominant spinocerebellar ataxia with sensory axonal neuropathy (SCA4): clinical description and genetic localization to chromosome 16q22.1K Flanigan, K Gardner, K Alderson, et al.
Cell|April 9, 1993
The elastin gene is disrupted by a translocation associated with supravalvular aortic stenosisM E Curran, D L Atkinson, A K Ewart, et al.
Diabetes|November 1, 1995
Linkage analysis of 19 candidate regions for insulin resistance in familial NIDDMS C Elbein, K C Chiu, M D Hoffman, et al.
Pageof 5

Showing results (11-20 of 49) with videos related to

Sort By:
Pageof 5
Neurology|May 1, 1992
Evidence of genetic heterogeneity among the nondystrophic myotoniasL J Ptacek, F A Ziter, J W Roberts, et al.
Diabetes|May 20, 1999
A genome-wide search for type 2 diabetes susceptibility genes in Utah CaucasiansS C Elbein, M D Hoffman, K Teng, et al.
Journal of Hypertension|March 22, 2000
Evaluation of heterodimeric guanylyl cyclase genes as candidates for human hypertensionR S Danziger, C Pappas, C Barnitz, et al.
Neuromuscular Disorders : NMD|August 30, 2001
Genetic characterization of a large, historically significant Utah kindred with facioscapulohumeral dystrophyK M Flanigan, C M Coffeen, L Sexton, et al.
Diabetes|March 1, 1996
Linkage studies of NIDDM with 23 chromosome 11 markers in a sample of whites of northern European descentS C Elbein, K L Bragg, M D Hoffman, et al.
The European Respiratory Journal|December 24, 1998
Factor V Leiden is not common in patients diagnosed with primary pulmonary hypertensionC G Elliott, M F Leppert, G J Alexander, et al.
The Western Journal of Medicine|October 1, 1987
Mapping approaches to gene identification in humansR L White, J M Lalouel, G M Lathrop, et al.
American Journal of Human Genetics|August 1, 1996
Autosomal dominant spinocerebellar ataxia with sensory axonal neuropathy (SCA4): clinical description and genetic localization to chromosome 16q22.1K Flanigan, K Gardner, K Alderson, et al.
Cell|April 9, 1993
The elastin gene is disrupted by a translocation associated with supravalvular aortic stenosisM E Curran, D L Atkinson, A K Ewart, et al.
Diabetes|November 1, 1995
Linkage analysis of 19 candidate regions for insulin resistance in familial NIDDMS C Elbein, K C Chiu, M D Hoffman, et al.
Pageof 5