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British Journal of Haematology
|
August 1, 1987
Characterization of a new alpha zero thalassaemia defect in the South African population
S Vandenplas, D R Higgs, R D Nicholls, et al.
Proceedings of the National Academy of Sciences of the United States of America
|
October 11, 2001
Identification of a conserved erythroid specific domain of histone acetylation across the alpha-globin gene cluster
E Anguita, C A Johnson, W G Wood, et al.
Australian Veterinary Journal
|
November 1, 1996
Anthrax in cattle in southern Western Australia
D Forshaw, A R Higgs, D C Moir, et al.
Lancet (London, England)
|
March 7, 1981
Molecular basis for mild forms of homozygous beta-thalassaemia
D J Weatherall, L Pressley, W G Wood, et al.
Clinical and Laboratory Haematology
|
November 26, 2005
Phenotype/genotype relationships in sickle cell disease: a pilot twin study
M W Weatherall, D R Higgs, H Weiss, et al.
ANZ Journal of Surgery
|
September 18, 2008
Surgical site marking does not affect sterility
John Rooney, Oliver K S Khoo, Andrew R Higgs, et al.
Nature
|
August 30, 1990
A truncated human chromosome 16 associated with alpha thalassaemia is stabilized by addition of telomeric repeat (TTAGGG)n
A O Wilkie, J Lamb, P C Harris, et al.
Gene
|
June 22, 2001
The human GPI1 gene is required for efficient glycosylphosphatidylinositol biosynthesis
A Tiede, R J Daniels, D R Higgs, et al.
Human Molecular Genetics
|
April 21, 2011
Functional significance of mutations in the Snf2 domain of ATRX
Matthew Mitson, Lawrence A Kelley, Michael J E Sternberg, et al.
British Journal of Haematology
|
May 1, 1980
Determination of alpha thalassaemia phenotypes by messenger RNA analysis
D M Hunt, D R Higgs, J B Clegg, et al.
Page
of 47
Search research articles
Search
Showing results (211-220 of 469) with videos related to
Sort By:
Page
of 47
British Journal of Haematology
|
August 1, 1987
Characterization of a new alpha zero thalassaemia defect in the South African population
S Vandenplas, D R Higgs, R D Nicholls, et al.
Proceedings of the National Academy of Sciences of the United States of America
|
October 11, 2001
Identification of a conserved erythroid specific domain of histone acetylation across the alpha-globin gene cluster
E Anguita, C A Johnson, W G Wood, et al.
Australian Veterinary Journal
|
November 1, 1996
Anthrax in cattle in southern Western Australia
D Forshaw, A R Higgs, D C Moir, et al.
Lancet (London, England)
|
March 7, 1981
Molecular basis for mild forms of homozygous beta-thalassaemia
D J Weatherall, L Pressley, W G Wood, et al.
Clinical and Laboratory Haematology
|
November 26, 2005
Phenotype/genotype relationships in sickle cell disease: a pilot twin study
M W Weatherall, D R Higgs, H Weiss, et al.
ANZ Journal of Surgery
|
September 18, 2008
Surgical site marking does not affect sterility
John Rooney, Oliver K S Khoo, Andrew R Higgs, et al.
Nature
|
August 30, 1990
A truncated human chromosome 16 associated with alpha thalassaemia is stabilized by addition of telomeric repeat (TTAGGG)n
A O Wilkie, J Lamb, P C Harris, et al.
Gene
|
June 22, 2001
The human GPI1 gene is required for efficient glycosylphosphatidylinositol biosynthesis
A Tiede, R J Daniels, D R Higgs, et al.
Human Molecular Genetics
|
April 21, 2011
Functional significance of mutations in the Snf2 domain of ATRX
Matthew Mitson, Lawrence A Kelley, Michael J E Sternberg, et al.
British Journal of Haematology
|
May 1, 1980
Determination of alpha thalassaemia phenotypes by messenger RNA analysis
D M Hunt, D R Higgs, J B Clegg, et al.
Page
of 47