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HbVar Database of Human Hemoglobin Variants and Thalassemia Mutations: 2007 Update
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HUMAN MUTATION (2007)
Haemoglobin E β thalassaemia in Sri Lanka
A Premawardhena et al.
LANCET (2005)
The Corfu δβ thalassemia deletion disrupts γ-globin gene silencing and reveals post-transcriptional regulation of HbF expression
L Chakalova et al.
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KML Gaensler et al.
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S de Silva et al.
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