Determinants of iron status and bilirubin levels in congenital dyserythropoietic anaemia type I

This publication has 10 references indexed in Scilit:

• Congenital dyserythropoiesis with intererythroblastic chromatin bridges and ultrastructurally-normal erythroblast heterochromatin: a new disorder
  British Journal of Haematology, 1998
• Congenital dyserythropoietic anaemias: clinical features, haematological morphology and new biochemical data
  Blood Reviews, 1998
• Haemochromatosis
  Clinical and Laboratory Haematology, 1998
• Hyperbilirubinaemia in heterozygous beta-thalassaemia is related to co-inherited Gilbert's syndrome.
  British Journal of Haematology, 1997
• The expression of uridine diphosphate glucuronosyltransferase gene is a major determinant of bilirubin level in heterozygous β‐thalassaemia and in glucose‐6‐phosphate dehydrogenase deficiency
  British Journal of Haematology, 1997
• Global prevalence of putative haemochromatosis mutations.
  Journal of Medical Genetics, 1997
• Genetic variation in bilirubin UDP-glucuronosyltransferase gene promoter and Gilbert's syndrome
  The Lancet, 1996
• The Genetic Basis of the Reduced Expression of Bilirubin UDP-Glucuronosyltransferase 1 in Gilbert's Syndrome
  New England Journal of Medicine, 1995
• Studies of erythroblast function in congenital dyserythropoietic anaemia, type I: evidence of impaired DNA, RNA, and protein synthesis and unbalanced globin chain synthesis in ultrastructurally abnormal cells.
  Journal of Clinical Pathology, 1986
• Clinical and Ultrastructural Aspects of Congenital Dyserythropoietic Anaemia Type I
  British Journal of Haematology, 1972