Detection of C282Y and H63D in the HFE gene. by Pointon, J, Merryweather-Clarke, A, Carella, M, Robson, K

Uncommon mutations and polymorphisms in the hemochromatosis gene. by Pointon, J, Wallace, D, Merryweather-Clarke, A, Robson, K

Geography of HFE C282Y and H63D mutations. by Merryweather-Clarke, A, Pointon, J, Jouanolle, A, Rochette, J, Robson, K

ESTIMATING DISEASE PENETRANCE IN P.C282Y HOMOZYGOTES IN THE UK by Bignell, P, Merryweather-Clarke, A, Lok, C, Schuh, A, Robson, K

COMPREHENSIVE GENETIC TESTING IS REQUIRED FOR PATIENTS WITH UNEXPLAINED IRON OVERLOAD by Bignell, P, Merryweather-Clarke, A, Lok, C, Schuh, A, Robson, K

A novel HFE mutation (c.del478) results in nonsense-mediated decay of the mutant transcript in a hemochromatosis patient. by Pointon, J, Lok, C, Shearman, J, Suckling, R, Rochette, J, Merryweather-Clarke, A, Robson, K

Juvenile haemochromatosis in the Bangladeshi community by Lok, C, Robins, A, Merryweather-Clarke, A, Hudson, J, Wai, P, Oleesky, D, Robson, K

Pilot study of early diagnosis of hereditary haemochromatosis through systematic case finding in primary care. by Emery, J, Rose, P, Harcourt, J, Livesey, K, Merryweather-Clarke, A, Pointon, J, Robson, K

Infertility: Consider haemochromatosis? by Lok, C, Gbegbaje, A, Mishra, B, Lipscomb, G, Hutchesson, A, Merryweather-Clarke, A, Robson, K

Expression of haemochromatosis-associated genes in the zebrafish by Lok, C, Merryweather-Clarke, A, Brakspear, K, Pinheiro, P, Patterson, L, Patient, R, Robson, K

GENE COMPARISON STUDIES OF ERYTHROBLASTS DERIVED FROM DIFFERENT HAEMATOPOIETIC SOURCES by Merryweather-Clarke, A, Lamikanra, A, Tsang, H, Yang, C, French, A, Carpenter, L, Watt, S, Roberts, D

Synergy between the C2 allele of transferrin and the C282Y allele of the haemochromatosis gene (HFE) as risk factors for developing Alzheimer's disease. by Robson, K, Lehmann, D, Wimhurst, V, Livesey, K, Combrinck, M, Merryweather-Clarke, A, Warden, DR, Smith, A

Recent advances in understanding haemochromatosis: a transition state. by Robson, K, Merryweather-Clarke, A, Cadet, E, Viprakasit, V, Zaahl, MG, Pointon, J, Weatherall, D, Rochette, J

Iron genes, iron load and risk of Alzheimer's disease. by Lehmann, D, Worwood, M, Ellis, R, Wimhurst, V, Merryweather-Clarke, A, Warden, DR, Smith, A, Robson, K

Hemochromatosis gene (HFE) mutations in South East Asia: a potential for iron overload. by Pointon, J, Viprakasit, V, Miles, K, Livesey, K, Steiner, M, O'Riordan, S, Hien, T, Merryweather-Clarke, A, Robson, K

Molecular diagnosis of the first ferroportin mutation (C326Y) in the far east causing a dominant form of inherited iron overload by Viprakasit, V, Merryweather-Clarke, A, Chinthammitr, Y, Schimanski, L, Drakesmith, H, Srichairatanakool, S, Limwongse, C, Townsend, A, Robson, K

A valine deletion of ferroportin 1: a common mutation in hemochromastosis type 4. by Roetto, A, Merryweather-Clarke, A, Daraio, F, Livesey, K, Pointon, J, Barbabietola, G, Piga, A, Mackie, P, Robson, K, Camaschella, C

A valine deletion of ferroportin 1: a common mutation in hemochromastosis type 4. by Roetto, A, Merryweather-Clarke, A, Daraio, F, Livesey, K, Pointon, J, Barbabietola, G, Piga, A, Mackie, P, Robson, K, Camaschella, C

In vitro binding of HFE to the cation-independent mannose-6 phosphate receptor. by Schimanski, L, Drakesmith, H, Sweetland, E, Bastin, J, Rezgui, D, Edelmann, M, Kessler, B, Merryweather-Clarke, A, Robson, K, Townsend, A

In vitro functional analysis of human ferroportin (FPN) and hemochromatosis-associated FPN mutations. by Schimanski, L, Drakesmith, H, Merryweather-Clarke, A, Viprakasit, V, Edwards, J, Sweetland, E, Bastin, J, Cowley, D, Chinthammitr, Y, Robson, K, Townsend, A