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E H Harley

Showing results (51-60 of 61) with videos related to

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British Journal of Haematology|September 1, 1983
The molecular basis of alpha thalassaemia in a South African populationC G Mathew, J Rousseau, J S Rees, et al.
The Journal of Clinical Investigation|September 1, 1988
Oxypurine cycle in human erythrocytes regulated by pH, inorganic phosphate, and oxygenP A Berman, D A Black, L Human, et al.
Journal of Inherited Metabolic Disease|January 1, 1990
Pyrimidine 5'-nucleotidase activity in normal and deficient human lymphoblastoid cellsD A Hopkinson, D M Swallow, A Marinaki, et al.
Intervirology|January 1, 1981
Characteristics of BK papovavirus DNA prepared directly from human urineR T Mew, G Lecatsas, O W Prozesky, et al.
Archives of Otolaryngology--Head & Neck Surgery|February 26, 1999
Birth trauma in the head and neckC A Hughes, E H Harley, G Milmoe, et al.
Journal of Inherited Metabolic Disease|January 1, 1996
Two siblings with episodic ketoacidosis and decreased activity of succinyl-CoA:3-ketoacid CoA-transferase in cultured fibroblastsC J Pretorius, G G Loy Son, F Bonnici, et al.
South African Medical Journal = Suid-Afrikaanse Tydskrif Vir Geneeskunde|February 18, 1984
Studies on cultured fibroblasts in a case of methylmalonic aciduriaJ S Davidson, A Lloyd, A Christianson, et al.
Clinica Chimica Acta; International Journal of Clinical Chemistry|February 15, 1988
Altered erythrocyte nucleotide patterns are characteristic of inherited disorders of purine or pyrimidine metabolismH A Simmonds, L D Fairbanks, G S Morris, et al.
Acta Haematologica|January 1, 1985
Incidence of Hb Barts and alpha-thalassaemia genotypes in a South African populationJ Rousseau, C G Mathew, J S Rees, et al.
Arteriosclerosis (Dallas, Tex.)|May 1, 1984
Low density lipoprotein receptor mutations in South African homozygous familial hypercholesterolemic patientsD R van der Westhuyzen, G A Coetzee, I P Demasius, et al.
Pageof 7

Showing results (51-60 of 61) with videos related to

Sort By:
Pageof 7
British Journal of Haematology|September 1, 1983
The molecular basis of alpha thalassaemia in a South African populationC G Mathew, J Rousseau, J S Rees, et al.
The Journal of Clinical Investigation|September 1, 1988
Oxypurine cycle in human erythrocytes regulated by pH, inorganic phosphate, and oxygenP A Berman, D A Black, L Human, et al.
Journal of Inherited Metabolic Disease|January 1, 1990
Pyrimidine 5'-nucleotidase activity in normal and deficient human lymphoblastoid cellsD A Hopkinson, D M Swallow, A Marinaki, et al.
Intervirology|January 1, 1981
Characteristics of BK papovavirus DNA prepared directly from human urineR T Mew, G Lecatsas, O W Prozesky, et al.
Archives of Otolaryngology--Head & Neck Surgery|February 26, 1999
Birth trauma in the head and neckC A Hughes, E H Harley, G Milmoe, et al.
Journal of Inherited Metabolic Disease|January 1, 1996
Two siblings with episodic ketoacidosis and decreased activity of succinyl-CoA:3-ketoacid CoA-transferase in cultured fibroblastsC J Pretorius, G G Loy Son, F Bonnici, et al.
South African Medical Journal = Suid-Afrikaanse Tydskrif Vir Geneeskunde|February 18, 1984
Studies on cultured fibroblasts in a case of methylmalonic aciduriaJ S Davidson, A Lloyd, A Christianson, et al.
Clinica Chimica Acta; International Journal of Clinical Chemistry|February 15, 1988
Altered erythrocyte nucleotide patterns are characteristic of inherited disorders of purine or pyrimidine metabolismH A Simmonds, L D Fairbanks, G S Morris, et al.
Acta Haematologica|January 1, 1985
Incidence of Hb Barts and alpha-thalassaemia genotypes in a South African populationJ Rousseau, C G Mathew, J S Rees, et al.
Arteriosclerosis (Dallas, Tex.)|May 1, 1984
Low density lipoprotein receptor mutations in South African homozygous familial hypercholesterolemic patientsD R van der Westhuyzen, G A Coetzee, I P Demasius, et al.
Pageof 7