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J E Craig

Showing results (11-20 of 53) with videos related to

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Bulletin of the New York Academy of Medicine|October 1, 1979
Private foundation health expenditures: a survey analysisJ E Craig, B L Dooley, D A Parker, et al.
British Journal of Haematology|December 1, 1992
Molecular characterization of a novel 10.3 kb deletion causing beta-thalassaemia with unusually high Hb A2J E Craig, S J Kelly, R Barnetson, et al.
American Journal of Ophthalmology|April 9, 2001
The Taa1 restriction enzyme provides a simple means to identify the Q368STOP mutation of the myocilin gene in primary open angle glaucomaP N Baird, J Dickinson, J E Craig, et al.
Blood|February 1, 1993
Rapid detection of a 13.4-kb deletion causing delta beta thalassemia in an Egyptian family by polymerase chain reactionJ E Craig, R Barnetson, D J Weatherall, et al.
British Journal of Haematology|May 1, 1993
The molecular basis of HPFH in a British family identified by heteroduplex formationJ E Craig, S M Sheerin, R Barnetson, et al.
Blood|February 15, 1995
Macedonian (delta beta) zero thalassemia has the same molecular basis as Turkish inversion-deletion (delta beta) zero thalassemiaJ E Craig, G D Efremov, C Fisher, et al.
Journal of Child Neurology|December 6, 2001
Genetic factors in athetoid cerebral palsyD J Amor, J E Craig, M B Delatycki, et al.
Journal of Bacteriology|December 11, 1997
A null mutation in the Bacillus subtilis aconitase gene causes a block in Spo0A-phosphate-dependent gene expressionJ E Craig, M J Ford, D C Blaydon, et al.
The Australian & New Zealand Journal of Obstetrics & Gynaecology|February 7, 2001
Low maternal serum oestriol at mid-trimester may indicate a fetal disorder of cholesterol biosynthesisJ E Craig, V Savage, D Cowley, et al.
Molecular Human Reproduction|March 2, 1999
No association between the -308 polymorphism in the tumour necrosis factor alpha (TNFalpha) promoter region and polycystic ovariesC R Milner, J E Craig, N D Hussey, et al.
Pageof 6

Showing results (11-20 of 53) with videos related to

Sort By:
Pageof 6
Bulletin of the New York Academy of Medicine|October 1, 1979
Private foundation health expenditures: a survey analysisJ E Craig, B L Dooley, D A Parker, et al.
British Journal of Haematology|December 1, 1992
Molecular characterization of a novel 10.3 kb deletion causing beta-thalassaemia with unusually high Hb A2J E Craig, S J Kelly, R Barnetson, et al.
American Journal of Ophthalmology|April 9, 2001
The Taa1 restriction enzyme provides a simple means to identify the Q368STOP mutation of the myocilin gene in primary open angle glaucomaP N Baird, J Dickinson, J E Craig, et al.
Blood|February 1, 1993
Rapid detection of a 13.4-kb deletion causing delta beta thalassemia in an Egyptian family by polymerase chain reactionJ E Craig, R Barnetson, D J Weatherall, et al.
British Journal of Haematology|May 1, 1993
The molecular basis of HPFH in a British family identified by heteroduplex formationJ E Craig, S M Sheerin, R Barnetson, et al.
Blood|February 15, 1995
Macedonian (delta beta) zero thalassemia has the same molecular basis as Turkish inversion-deletion (delta beta) zero thalassemiaJ E Craig, G D Efremov, C Fisher, et al.
Journal of Child Neurology|December 6, 2001
Genetic factors in athetoid cerebral palsyD J Amor, J E Craig, M B Delatycki, et al.
Journal of Bacteriology|December 11, 1997
A null mutation in the Bacillus subtilis aconitase gene causes a block in Spo0A-phosphate-dependent gene expressionJ E Craig, M J Ford, D C Blaydon, et al.
The Australian & New Zealand Journal of Obstetrics & Gynaecology|February 7, 2001
Low maternal serum oestriol at mid-trimester may indicate a fetal disorder of cholesterol biosynthesisJ E Craig, V Savage, D Cowley, et al.
Molecular Human Reproduction|March 2, 1999
No association between the -308 polymorphism in the tumour necrosis factor alpha (TNFalpha) promoter region and polycystic ovariesC R Milner, J E Craig, N D Hussey, et al.
Pageof 6