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Human Mutation|January 1, 1997
Mutations in mut methylmalonic acidemia: clinical and enzymatic correlationsF D Ledley, D S RosenblattBulletin De L'Academie Nationale De Medecine|October 1, 1996
[A molecular study of methylmalonic aciduria: structure-function correlations]D S Rosenblatt, F D LedleyAmerican Journal of Medical Genetics|March 1, 1993
Varying neurological phenotypes among muto and mut- patients with methylmalonylCoA mutase deficiencyM I Shevell, N Matiaszuk, F D Ledley, et al.The Journal of Clinical Investigation|January 1, 1991
Genetic characterization of a MUT locus mutation discriminating heterogeneity in mut0 and mut- methylmalonic aciduria by interallelic complementationM L Raff, A M Crane, R Jansen, et al.The Journal of Clinical Investigation|April 1, 1994
Cloning and expression of mutations demonstrating intragenic complementation in mut0 methylmalonic aciduriaA A Qureshi, A M Crane, N V Matiaszuk, et al.Proceedings of the National Academy of Sciences of the United States of America|May 28, 1996
Molecular basis for dysfunction of some mutant forms of methylmalonyl-CoA mutase: deductions from the structure of methionine synthaseC L Drennan, R G Matthews, D S Rosenblatt, et al.Clinical and Investigative Medicine. Medecine Clinique Et Experimentale|December 1, 1992
The quality of medical scienceF D LedleyThe Journal of Investigative Dermatology|November 1, 1994
Therapeutic promise of molecular geneticsF D LedleyClinical and Investigative Medicine. Medecine Clinique Et Experimentale|February 1, 1993
Are contemporary methods for somatic gene therapy suitable for clinical applications?F D LedleyEuropean Journal of Pediatrics|September 1, 1991
Clinical application of genotypic diagnosis for phenylketonuria: theoretical considerationsF D LedleyPageof 19