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Clinical and Laboratory Haematology
|
January 1, 1981
Ultrastructure of red cells containing haemoglobin H inclusions induced by redox dyes
S N Wickramasinghe, M Hughes, D R Higgs, et al.
The American Journal of Medicine
|
August 1, 1983
Clinical features and molecular analysis of acquired hemoglobin H disease
D R Higgs, W G Wood, C Barton, et al.
The Journal of Pediatrics
|
June 1, 1985
Clinical presentation of homozygous sickle cell disease
R Bainbridge, D R Higgs, G H Maude, et al.
Cell
|
October 1, 1985
Recombination within the human embryonic xi-globin locus: a common xi-xi chromosome produced by gene conversion of the psi xi gene
A V Hill, R D Nicholls, S L Thein, et al.
British Journal of Haematology
|
September 1, 1981
A new triplicated alpha-globin gene arrangement in man
R J Trent, D R Higgs, J B Clegg, et al.
Mammalian Genome : Official Journal of the International Mammalian Genome Society
|
May 8, 1998
Comparison of the human and murine ATRX gene identifies highly conserved, functionally important domains
D J Picketts, A O Tastan, D R Higgs, et al.
Blood
|
June 1, 1985
Alpha zero-thalassemia due to recombination between the alpha 1-globin gene and an AluI repeat
R D Nicholls, D R Higgs, J B Clegg, et al.
Proceedings of the National Academy of Sciences of the United States of America
|
August 1, 1983
Molecular basis of length polymorphism in the human zeta-globin gene complex
S E Goodbourn, D R Higgs, J B Clegg, et al.
Journal of Medical Genetics
|
August 1, 1979
G gamma beta + type of hereditary persistence of fetal haemoglobin in association with Hb C
D R Higgs, J B Clegg, W G Wood, et al.
European Journal of Haematology
|
February 1, 1990
Alpha thalassaemia in two Spanish families
A Villegas, F Calero, M A Vickers, et al.
Page
of 19
Search research articles
Search
Showing results (41-50 of 183) with videos related to
Sort By:
Page
of 19
Clinical and Laboratory Haematology
|
January 1, 1981
Ultrastructure of red cells containing haemoglobin H inclusions induced by redox dyes
S N Wickramasinghe, M Hughes, D R Higgs, et al.
The American Journal of Medicine
|
August 1, 1983
Clinical features and molecular analysis of acquired hemoglobin H disease
D R Higgs, W G Wood, C Barton, et al.
The Journal of Pediatrics
|
June 1, 1985
Clinical presentation of homozygous sickle cell disease
R Bainbridge, D R Higgs, G H Maude, et al.
Cell
|
October 1, 1985
Recombination within the human embryonic xi-globin locus: a common xi-xi chromosome produced by gene conversion of the psi xi gene
A V Hill, R D Nicholls, S L Thein, et al.
British Journal of Haematology
|
September 1, 1981
A new triplicated alpha-globin gene arrangement in man
R J Trent, D R Higgs, J B Clegg, et al.
Mammalian Genome : Official Journal of the International Mammalian Genome Society
|
May 8, 1998
Comparison of the human and murine ATRX gene identifies highly conserved, functionally important domains
D J Picketts, A O Tastan, D R Higgs, et al.
Blood
|
June 1, 1985
Alpha zero-thalassemia due to recombination between the alpha 1-globin gene and an AluI repeat
R D Nicholls, D R Higgs, J B Clegg, et al.
Proceedings of the National Academy of Sciences of the United States of America
|
August 1, 1983
Molecular basis of length polymorphism in the human zeta-globin gene complex
S E Goodbourn, D R Higgs, J B Clegg, et al.
Journal of Medical Genetics
|
August 1, 1979
G gamma beta + type of hereditary persistence of fetal haemoglobin in association with Hb C
D R Higgs, J B Clegg, W G Wood, et al.
European Journal of Haematology
|
February 1, 1990
Alpha thalassaemia in two Spanish families
A Villegas, F Calero, M A Vickers, et al.
Page
of 19