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Lancet (London, England)|December 12, 2003
Screening for hereditary haemochromatosis within families and beyondC Anne McCune, David Ravine, Mark Worwood, et al.
Haematologica|February 16, 2005
Changes in erythropoiesis in hereditary hemochromatosis are not mediated by HFE expression in nucleated red cellsGraham P Feeney, Kymberley Carter, Gillian S Masters, et al.
Haematologica|February 8, 2006
The limited value of methylmalonic acid, homocysteine and holotranscobalamin in the diagnosis of early B12 deficiencyAndrew Goringe, Richard Ellis, Ian McDowell, et al.
Clinical Chemistry and Laboratory Medicine|October 11, 2008
Automated immunoassay methods for ferritin: recovery studies to assess traceability to an international standardSheena Blackmore, Malcolm Hamilton, Anne Lee, et al.
Human Genetics|August 4, 2004
The origin and spread of the HFE-C282Y haemochromatosis mutationS Distante, K J H Robson, J Graham-Campbell, et al.
Pediatric Blood & Cancer|August 28, 2009
Hereditary hemochromatosis gene (HFE) variants are associated with birth weight and childhood leukemia riskM Tevfik Dorak, Rachel K Mackay, Caroline L Relton, et al.
Human Genetics|November 19, 2002
Hereditary haemochromatosis: only 1% of adult HFEC282Y homozygotes in South Wales have a clinical diagnosis of iron overloadC Anne McCune, Layla N Al-Jader, Alison May, et al.
Blood|July 2, 2002
Autosomal dominant reticuloendothelial iron overload associated with a 3-base pair deletion in the ferroportin 1 gene (SLC11A3)Vinod Devalia, Kymberley Carter, Ann P Walker, et al.
The American Journal of Clinical Nutrition|October 8, 2005
Diet and genetic factors associated with iron status in middle-aged womenJanet E Cade, Jennifer A Moreton, Beverley O'Hara, et al.
The British Journal of Nutrition|October 3, 2006
Risk of iron overload in carriers of genetic mutations associated with hereditary haemochromatosis: UK Food Standards Agency workshopMamta Singh, Margaret Ashwell, Peter Sanderson, et al.
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