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G B MacPhee

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Journal of Inherited Metabolic Disease|January 1, 1984
Infantile type 2 sialidosis in a Pakistani family--a clinical and biochemical studyM King, F Cockburn, G B MacPhee, et al.
Clinica Chimica Acta; International Journal of Clinical Chemistry|February 28, 1990
A new sensitive microassay for the measurement of erythrocyte glycogenJ Farquharson, E C Jamieson, G B MacPhee, et al.
Archives of Disease in Childhood|October 1, 1993
Malonyl coenzyme A decarboxylase deficiencyG B MacPhee, R W Logan, J S Mitchell, et al.
Pageof 1

Showing results (1-10 of 3) with videos related to

Sort By:
Pageof 1
Journal of Inherited Metabolic Disease|January 1, 1984
Infantile type 2 sialidosis in a Pakistani family--a clinical and biochemical studyM King, F Cockburn, G B MacPhee, et al.
Clinica Chimica Acta; International Journal of Clinical Chemistry|February 28, 1990
A new sensitive microassay for the measurement of erythrocyte glycogenJ Farquharson, E C Jamieson, G B MacPhee, et al.
Archives of Disease in Childhood|October 1, 1993
Malonyl coenzyme A decarboxylase deficiencyG B MacPhee, R W Logan, J S Mitchell, et al.
Pageof 1