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D R Higgs

Showing results (41-50 of 183) with videos related to

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Clinical and Laboratory Haematology|January 1, 1981
Ultrastructure of red cells containing haemoglobin H inclusions induced by redox dyesS 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 diseaseD R Higgs, W G Wood, C Barton, et al.
The Journal of Pediatrics|June 1, 1985
Clinical presentation of homozygous sickle cell diseaseR 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 geneA 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 manR 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 domainsD 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 repeatR 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 complexS 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 CD R Higgs, J B Clegg, W G Wood, et al.
European Journal of Haematology|February 1, 1990
Alpha thalassaemia in two Spanish familiesA Villegas, F Calero, M A Vickers, et al.
Pageof 19

Showing results (41-50 of 183) with videos related to

Sort By:
Pageof 19
Clinical and Laboratory Haematology|January 1, 1981
Ultrastructure of red cells containing haemoglobin H inclusions induced by redox dyesS 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 diseaseD R Higgs, W G Wood, C Barton, et al.
The Journal of Pediatrics|June 1, 1985
Clinical presentation of homozygous sickle cell diseaseR 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 geneA 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 manR 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 domainsD 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 repeatR 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 complexS 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 CD R Higgs, J B Clegg, W G Wood, et al.
European Journal of Haematology|February 1, 1990
Alpha thalassaemia in two Spanish familiesA Villegas, F Calero, M A Vickers, et al.
Pageof 19