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Journal of the Royal Society of Medicine
|
March 18, 2008
William Bateson, the rediscoverer of Mendel
Milo Keynes, T M Cox
American Journal of Human Genetics
|
April 1, 1995
Diverse mutations in the aldolase B gene that underlie the prevalence of hereditary fructose intolerance
M Ali, T M Cox
Journal of the Royal College of Physicians of London
|
April 1, 1993
The MB PhD programme. Training to be a clinician-scientist in the UK
T M Cox, R Wakeford
Journal of Medical Genetics
|
November 1, 1993
The glucocerebrosidase locus in Gaucher's disease: molecular analysis of a lysosomal enzyme
P K Mistry, T M Cox
The Journal of Biological Chemistry
|
January 14, 1994
Purple acid phosphatase of the human macrophage and osteoclast. Characterization, molecular properties, and crystallization of the recombinant di-iron-oxo protein secreted by baculovirus-infected insect cells
A R Hayman, T M Cox
American Journal of Human Genetics
|
July 1, 1990
Partial aldolase B gene deletions in hereditary fructose intolerance
N C Cross, T M Cox
European Journal of Haematology
|
February 1, 1989
Hereditary haemochromatosis
T M Cox, D K Lord
Bailliere'S Clinical Haematology
|
March 14, 1998
Gaucher's disease: clinical features and natural history
T M Cox, J P Schofield
British Journal of Haematology
|
January 1, 1980
Cellular mechanisms in the regulation of iron absorption by the human intestine: studies in patients with iron deficiency before and after treatment
T M Cox, T J Peters
The Journal of Biological Chemistry
|
May 15, 1988
Biosynthesis of heme in immature erythroid cells. The regulatory step for heme formation in the human erythron
L C Gardner, T M Cox
Page
of 15
Search research articles
Search
Showing results (21-30 of 146) with videos related to
Sort By:
Page
of 15
Journal of the Royal Society of Medicine
|
March 18, 2008
William Bateson, the rediscoverer of Mendel
Milo Keynes, T M Cox
American Journal of Human Genetics
|
April 1, 1995
Diverse mutations in the aldolase B gene that underlie the prevalence of hereditary fructose intolerance
M Ali, T M Cox
Journal of the Royal College of Physicians of London
|
April 1, 1993
The MB PhD programme. Training to be a clinician-scientist in the UK
T M Cox, R Wakeford
Journal of Medical Genetics
|
November 1, 1993
The glucocerebrosidase locus in Gaucher's disease: molecular analysis of a lysosomal enzyme
P K Mistry, T M Cox
The Journal of Biological Chemistry
|
January 14, 1994
Purple acid phosphatase of the human macrophage and osteoclast. Characterization, molecular properties, and crystallization of the recombinant di-iron-oxo protein secreted by baculovirus-infected insect cells
A R Hayman, T M Cox
American Journal of Human Genetics
|
July 1, 1990
Partial aldolase B gene deletions in hereditary fructose intolerance
N C Cross, T M Cox
European Journal of Haematology
|
February 1, 1989
Hereditary haemochromatosis
T M Cox, D K Lord
Bailliere'S Clinical Haematology
|
March 14, 1998
Gaucher's disease: clinical features and natural history
T M Cox, J P Schofield
British Journal of Haematology
|
January 1, 1980
Cellular mechanisms in the regulation of iron absorption by the human intestine: studies in patients with iron deficiency before and after treatment
T M Cox, T J Peters
The Journal of Biological Chemistry
|
May 15, 1988
Biosynthesis of heme in immature erythroid cells. The regulatory step for heme formation in the human erythron
L C Gardner, T M Cox
Page
of 15