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I B Sardharwalla

Showing results (1-10 of 37) with videos related to

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The Nursing Journal of India|August 1, 1988
Workshop for trainers of TBAsI B Sardharwalla
Archives of Disease in Childhood|September 1, 1974
Proceedings: Case of hyperammonaemia due to ornithine transcarbamylase deficiencyC Morley, I B Sardharwalla
Archives of Disease in Childhood|February 1, 1972
Plasma levels of cystine in homocystinuriaI B Sardharwalla, B Fowler
Archives of Disease in Childhood|November 1, 1984
Coagulation defect of congenital tyrosinaemiaD I Evans, I B Sardharwalla
Monographs in Human Genetics|January 1, 1978
A new type of heterozygote of familial renal iminoglycinuriaE A Law, I B Sardharwalla
British Medical Journal|August 19, 1972
Screening for inherited metabolic diseasesG M Komrower, I B Sardharwalla
Nutrition and Health|January 1, 1987
GalactosaemiaI B Sardharwalla, J E Wraith
Journal 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 Wraith
The Biochemical Journal|March 1, 1971
The detection of heterozygotes for homocystinuria by oral loading with L-methionineB Fowler, I B Sardharwalla, A J Robins
Journal 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 Sardharwalla
Pageof 4

Showing results (1-10 of 37) with videos related to

Sort By:
Pageof 4
The Nursing Journal of India|August 1, 1988
Workshop for trainers of TBAsI B Sardharwalla
Archives of Disease in Childhood|September 1, 1974
Proceedings: Case of hyperammonaemia due to ornithine transcarbamylase deficiencyC Morley, I B Sardharwalla
Archives of Disease in Childhood|February 1, 1972
Plasma levels of cystine in homocystinuriaI B Sardharwalla, B Fowler
Archives of Disease in Childhood|November 1, 1984
Coagulation defect of congenital tyrosinaemiaD I Evans, I B Sardharwalla
Monographs in Human Genetics|January 1, 1978
A new type of heterozygote of familial renal iminoglycinuriaE A Law, I B Sardharwalla
British Medical Journal|August 19, 1972
Screening for inherited metabolic diseasesG M Komrower, I B Sardharwalla
Nutrition and Health|January 1, 1987
GalactosaemiaI B Sardharwalla, J E Wraith
Journal 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 Wraith
The Biochemical Journal|March 1, 1971
The detection of heterozygotes for homocystinuria by oral loading with L-methionineB Fowler, I B Sardharwalla, A J Robins
Journal 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 Sardharwalla
Pageof 4