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British Medical Journal|September 15, 1979
The Manchester regional screening programme: a 10-year exercise in patient and family careG M Komrower, I B Sardharwalla, B Fowler, et al.British Medical Journal|May 26, 1979
Management of maternal phenylketonuria: an emerging clinical problemG M Komrower, I B Sardharwalla, J M Coutts, et al.Archives of Disease in Childhood|November 1, 1984
Coagulation defect of congenital tyrosinaemiaD I Evans, I B SardharwallaJournal of Inherited Metabolic Disease|January 1, 1989
A clinician's view of the mass screening of the newborn for inherited diseases: current practice and future considerationsI B Sardharwalla, J E WraithJournal of Inherited Metabolic Disease|January 1, 1987
Acid beta-mannosidase of human plasma: influence of age and sex on enzyme activityA Cooper, C Hatton, I B SardharwallaJournal of Inherited Metabolic Disease|January 1, 1989
Chorionic villus sampling: diagnostic uses and limitations of enzyme assaysB Fowler, L Giles, A Cooper, et al.Journal of Inherited Metabolic Disease|January 1, 1988
Human beta-mannosidase deficiency: biochemical findings in plasma, fibroblasts, white cells and urineA Cooper, C Hatton, M Thornley, et al.Prenatal Diagnosis|March 1, 1988
First trimester prenatal diagnosis of Sandhoff's diseaseL Giles, A Cooper, B Fowler, et al.Journal of Inherited Metabolic Disease|January 1, 1990
Alpha- and beta-mannosidosesA Cooper, C E Hatton, M Thornley, et al.Pageof 3