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Prenatal Diagnosis|February 1, 1991
Detection of fetal cells in maternal bloodS C Yeoh, I L Sargent, C W Redman, et al.British Journal of Haematology|February 5, 1998
Beta-thalassaemia intermedia: is it possible consistently to predict phenotype from genotype?P J Ho, G W Hall, L Y Luo, et al.Journal of Medical Genetics|December 1, 1985
Prenatal diagnosis of the common haemoglobin disordersD J Weatherall, J M Old, S L Thein, et al.Gut|August 1, 1973
Inheritance and influence of histocompatibility (HL-A) antigens in adult coeliac diseaseP L Stokes, P Asquith, G K Holmes, et al.British Journal of Haematology|July 1, 1991
A novel delta 0 mutation in cis with Hb Knossos: a study of different genetic interactions in three Egyptian familiesR J Olds, T Sura, B Jackson, et al.Blood|December 3, 1998
Recombination breakpoints in the human beta-globin gene clusterR A Smith, P J Ho, J B Clegg, et al.Lancet (London, England)|December 1, 1979
Is faecal alpha 1-antitrypsin excretion a reliable screening test for protein-losing enteropathy?M R Haeney, J Fields, R A Carter, et al.Journal of Clinical Pathology|March 1, 1982
Soya protein antibodies in man: their occurrence and possible relevance in coeliac diseaseM R Haeney, B J Goodwin, M E Barratt, et al.British Medical Journal|February 10, 1973
Serum alkaline phosphatase and rickets in urban schoolchildrenW T Cooke, C H Swan, P Asquith, et al.British Journal of Haematology|June 1, 1984
Population and genetic studies suggest a single origin for the Indian deletion beta thalassaemiaS L Thein, J M Old, J S Wainscoat, et al.Pageof 15