Ian Hambleton
Ian Hambleton
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"Sickle Cell/genetics/mortality/physiopathology"
Hb S-β-thalassemia: molecular, hematological and clinical comparisons.
Clinical and hematological features are presented for 261 patients with identified β-thalassemia (β-thal) mutations. Mutations causing …
Graham R. Serjeant
,
Beryl E. Serjeant
,
Raphael A. Fraser
,
Ian R. Hambleton
,
Douglas R. Higgs
,
Andreas E. Kulozik
,
Alan Donaldson
Cite
DOI
Hb S-β-thalassemia: molecular, hematological and clinical comparisons.
Clinical and hematological features are presented for 261 patients with identified β-thalassemia (β-thal) mutations. Mutations causing …
Graham R. Serjeant
,
Beryl E. Serjeant
,
Raphael A. Fraser
,
Ian R. Hambleton
,
Douglas R. Higgs
,
Andreas E. Kulozik
,
Alan Donaldson
Cite
DOI
Hb S-β-thalassemia: molecular, hematological and clinical comparisons.
Clinical and hematological features are presented for 261 patients with identified β-thalassemia (β-thal) mutations. Mutations causing …
Graham R. Serjeant
,
Beryl E. Serjeant
,
Raphael A. Fraser
,
Ian R. Hambleton
,
Douglas R. Higgs
,
Andreas E. Kulozik
,
Alan Donaldson
Cite
DOI
Hb S-β-thalassemia: molecular, hematological and clinical comparisons.
Clinical and hematological features are presented for 261 patients with identified β-thalassemia (β-thal) mutations. Mutations causing …
Graham R. Serjeant
,
Beryl E. Serjeant
,
Raphael A. Fraser
,
Ian R. Hambleton
,
Douglas R. Higgs
,
Andreas E. Kulozik
,
Alan Donaldson
Cite
DOI
Cite
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