Ten novel mutations in the erythroid transcription factor KLF1 gene associated with increased fetal hemoglobin levels in adults. by Gallienne, A, Dréau, H, Schuh, A, Old, J, Henderson, S

Nine Novel Mutations in the Erythroid Transcription Factor KLF1 Gene Associated with Increased Fetal Hemoglobin Levels in Adults by Gallienne, A, Dreau, H, Schuh, A, Hatton, C, Old, J, Henderson, S

Application of MLPA and gap-PCR mapping to characterise a novel beta globin gene cluster deletion mutation in a family of Afghan ancestry by Gallienne, A, Hampson, J, Bignell, P, Old, J, Schuh, A, Henderson, S

A study of δ-globin gene mutations in the UK population: identification of three novel variants and development of a novel DNA test for Hb A'2. by Khalil, MS, Marouf, S, Element, D, Timbs, A, Gallienne, A, Schuh, A, Old, J, Henderson, S

Characterization of a novel deletion causing beta-thalassemia major in an Afghan family. by Gallienne, A, Iberson, N, Dréau, H, Jackson, H, Bignell, P, Old, J, Schuh, A, Henderson, S

Multiplex ligation-dependent probe amplification identification of 17 different beta-globin gene deletions (including four novel mutations) in the UK population. by Gallienne, A, Dréau, H, McCarthy, J, Timbs, A, Hampson, J, Schuh, A, Old, J, Henderson, S

Incidence of haemoglobinopathies in various populations - the impact of immigration. by Henderson, S, Timbs, A, McCarthy, J, Gallienne, A, Van Mourik, M, Masters, G, May, A, Khalil, MS, Schuh, A, Old, J