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P M George

Showing results (111-120 of 165) with videos related to

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British Journal of Haematology|May 1, 1992
A family with haemolytic anaemia and three beta-globins: the deletion in haemoglobin Atlanta-Coventry (beta 75 Leu----Pro, 141 Leu deleted) is not present at the nucleotide levelP M George, T Myles, D Williamson, et al.
Neuroscience Letters|April 21, 1995
Superoxide dismutase (glu100-->gly) in a family with inherited motor neuron disease: detection of mutant superoxide dismutase activity and the presence of heterodimersV L Calder, N M Domigan, P M George, et al.
Annals of Clinical Biochemistry|October 23, 2008
Three cases of congenital adrenal hypoplasia with novel mutations in the (NROB1) DAX-1 geneB Wheeler, P M George, K Mackenzie, et al.
Annals of Clinical Biochemistry|September 14, 2002
Macro-alkaline phosphatase due to IgG kappa complex: demonstration with polyethylene glycol precipitation and immunofixationM C Owen, L S Pike, P M George, et al.
Australian and New Zealand Journal of Medicine|August 1, 1993
Concurrent hepatitis B and C infection treated successfully with alpha interferonM J Burt, B A Chapman, B J Scrimshaw, et al.
Pathology|January 1, 2015
Hazards of a floating separator gel: a case studyJ B Ryan, S J Southby, L A Stuart, et al.
Clinical Chemistry|February 5, 2000
Correction for Stott et al.: simple multiplex PCR for the simultaneous detection of the C282Y and H63D hemochromatosis (HFE) gene mutationsM K Stott, A P Fellowes, J D Upton, et al.
Molecular Pathology : MP|April 8, 1999
Identification of a novel PTEN mutation (L139X) in a patient with Cowden disease and Sjögren's syndromeA M Raizis, M M Ferguson, B A Robinson, et al.
Pathology|December 24, 2005
Autosomal recessive adult-onset hypophosphatasiaJ R Harraway, J M Sheard, S J Soule, et al.
The Journal of Clinical Investigation|August 1, 1988
Cleavage and inactivation of alpha 1-antitrypsin by metalloproteinases released from neutrophilsM C Vissers, P M George, I C Bathurst, et al.
Pageof 17

Showing results (111-120 of 165) with videos related to

Sort By:
Pageof 17
British Journal of Haematology|May 1, 1992
A family with haemolytic anaemia and three beta-globins: the deletion in haemoglobin Atlanta-Coventry (beta 75 Leu----Pro, 141 Leu deleted) is not present at the nucleotide levelP M George, T Myles, D Williamson, et al.
Neuroscience Letters|April 21, 1995
Superoxide dismutase (glu100-->gly) in a family with inherited motor neuron disease: detection of mutant superoxide dismutase activity and the presence of heterodimersV L Calder, N M Domigan, P M George, et al.
Annals of Clinical Biochemistry|October 23, 2008
Three cases of congenital adrenal hypoplasia with novel mutations in the (NROB1) DAX-1 geneB Wheeler, P M George, K Mackenzie, et al.
Annals of Clinical Biochemistry|September 14, 2002
Macro-alkaline phosphatase due to IgG kappa complex: demonstration with polyethylene glycol precipitation and immunofixationM C Owen, L S Pike, P M George, et al.
Australian and New Zealand Journal of Medicine|August 1, 1993
Concurrent hepatitis B and C infection treated successfully with alpha interferonM J Burt, B A Chapman, B J Scrimshaw, et al.
Pathology|January 1, 2015
Hazards of a floating separator gel: a case studyJ B Ryan, S J Southby, L A Stuart, et al.
Clinical Chemistry|February 5, 2000
Correction for Stott et al.: simple multiplex PCR for the simultaneous detection of the C282Y and H63D hemochromatosis (HFE) gene mutationsM K Stott, A P Fellowes, J D Upton, et al.
Molecular Pathology : MP|April 8, 1999
Identification of a novel PTEN mutation (L139X) in a patient with Cowden disease and Sjögren's syndromeA M Raizis, M M Ferguson, B A Robinson, et al.
Pathology|December 24, 2005
Autosomal recessive adult-onset hypophosphatasiaJ R Harraway, J M Sheard, S J Soule, et al.
The Journal of Clinical Investigation|August 1, 1988
Cleavage and inactivation of alpha 1-antitrypsin by metalloproteinases released from neutrophilsM C Vissers, P M George, I C Bathurst, et al.
Pageof 17