Contact information
Research groups
Chris Fisher
Diagnostic Laboratory Manager
Recent publications
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Hepcidin is suppressed by erythropoiesis in hemoglobin E β-thalassemia and β-thalassemia trait.
Journal article
Jones E. et al, (2015), Blood, 125, 873 - 880
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Rare hemoglobin variants: Hb G-Szuhu (HBB: c.243C>G), Hb G-Coushatta (HBB: c.68A>C) and Hb Mizuho (HBB: c.206T>C) in Sri Lankan families.
Journal article
Perera PS. et al, (2015), Hemoglobin, 39, 62 - 65
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A novel molecular basis for β thalassemia intermedia poses new questions about its pathophysiology (Blood (2005) 106, 9 (3251-3255))
Journal article
Premawardhena A. et al, (2011), Blood, 118
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First case of dizygous twins with X-linked alpha-thalassemia/mental retardation syndrome showing wide clinical variability.
Journal article
Pavone P. et al, (2010), Pediatr Int, 52, e72 - e75
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Identification of three novel mutations [-41 (A>C), codon 24 (-G), and IVS-I-109 (-T)], in a study of beta-thalassemia alleles in the Isfahan region of Iran.
Journal article
Salehi R. et al, (2010), Hemoglobin, 34, 115 - 120