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T W Prior

Showing results (1-10 of 75) with videos related to

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Clinical Chemistry|April 29, 1998
Determining gene dosageT W Prior
Clinics in Laboratory Medicine|December 1, 1995
Perspectives and molecular diagnosis of Duchenne and Becker muscular dystrophiesT W Prior
Archives of Pathology & Laboratory Medicine|October 1, 1991
Genetic analysis of the Duchenne muscular dystrophy geneT W Prior
Seminars in Neurology|January 1, 1997
Issues related to DNA testing for Huntington's disease in symptomatic patientsG W Paulson, T W Prior
Journal of Child Neurology|March 1, 1995
The childhood muscular dystrophies: diseases sharing a common pathogenesis of membrane instabilityJ R Mendell, Z Sahenk, T W Prior
Current Opinion in Neurology|October 1, 1994
The impact of molecular genetics on the care of patients with muscle diseaseN Nadkarni, T W Prior, J R Mendell
American Journal of Medical Genetics|October 21, 1998
Identification of a missense mutation in a Friedreich's ataxia patient: implications for diagnosis and carrier studiesC Bartolo, J R Mendell, T W Prior
Clinical Chemistry|June 1, 1989
Detection of Duchenne/Becker muscular dystrophy carriers by densitometric scanningT W Prior, K J Friedman, L M Silverman
Nucleic Acids Research|March 25, 1989
RFLP for HindIII at the Duchenne muscular dystrophy geneT W Prior, K J Friedman, L M Silverman
Annals of Clinical and Laboratory Science|March 1, 1989
Sensitivity of serum fructosamine in short term glycemic controlT W Prior, J F Chapman, D D Bankson
Pageof 8

Showing results (1-10 of 75) with videos related to

Sort By:
Pageof 8
Clinical Chemistry|April 29, 1998
Determining gene dosageT W Prior
Clinics in Laboratory Medicine|December 1, 1995
Perspectives and molecular diagnosis of Duchenne and Becker muscular dystrophiesT W Prior
Archives of Pathology & Laboratory Medicine|October 1, 1991
Genetic analysis of the Duchenne muscular dystrophy geneT W Prior
Seminars in Neurology|January 1, 1997
Issues related to DNA testing for Huntington's disease in symptomatic patientsG W Paulson, T W Prior
Journal of Child Neurology|March 1, 1995
The childhood muscular dystrophies: diseases sharing a common pathogenesis of membrane instabilityJ R Mendell, Z Sahenk, T W Prior
Current Opinion in Neurology|October 1, 1994
The impact of molecular genetics on the care of patients with muscle diseaseN Nadkarni, T W Prior, J R Mendell
American Journal of Medical Genetics|October 21, 1998
Identification of a missense mutation in a Friedreich's ataxia patient: implications for diagnosis and carrier studiesC Bartolo, J R Mendell, T W Prior
Clinical Chemistry|June 1, 1989
Detection of Duchenne/Becker muscular dystrophy carriers by densitometric scanningT W Prior, K J Friedman, L M Silverman
Nucleic Acids Research|March 25, 1989
RFLP for HindIII at the Duchenne muscular dystrophy geneT W Prior, K J Friedman, L M Silverman
Annals of Clinical and Laboratory Science|March 1, 1989
Sensitivity of serum fructosamine in short term glycemic controlT W Prior, J F Chapman, D D Bankson
Pageof 8