Search Results - Dover, G.J.

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  1. 1
    Fetal Hemoglobin Levels in Sickle Cell Disease and Normal Individuals Are Partially Controlled by an X-Linked Gene Located at Xp22.2

    Fetal Hemoglobin Levels in Sickle Cell Disease and Normal Individuals Are Partially Controlled by an X-Linked Gene Located at Xp22.2 by Dover, G.J., Smith, K.D., Chang, Y.C., Purvis, S., Mays, A., Meyers, D.A., Sheils, C., Serjeant, G.

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  2. 2
    An Analysis of Fetal Hemoglobin Variation in Sickle Cell Disease: The Relative Contributions of the X-Linked Factor, β-Globin Haplotypes, α-Globin Gene Number, Gender, and Age

    An Analysis of Fetal Hemoglobin Variation in Sickle Cell Disease: The Relative Contributions of the X-Linked Factor, β-Globin Haplotypes, α-Globin Gene Number, Gender, and Age by Chang, Y.C., Smith, K.D., Moore, R.D., Serjeant, G.R., Dover, G.J.

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  3. 3
    Hydroxyurea Induction of Hemoglobin F Production in Sickle Cell Disease: Relationship Between Cytotoxicity and F Cell Production

    Hydroxyurea Induction of Hemoglobin F Production in Sickle Cell Disease: Relationship Between Cytotoxicity and F Cell Production by Dover, G.J., Humphries, R.K., Moore, J.G., Ley, T.J., Young, N.S., Charache, S., Nienhuis, A.W.

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  4. 4
    Dinucleotide repeat polymorphisms at the DXS85, DXS16 and DXS43 loci

    Dinucleotide repeat polymorphisms at the DXS85, DXS16 and DXS43 loci by Chang, Y.-P.C., Smith, K.D., Dover, G.J.

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  5. 5
    Variation in Hemoglobin F Production Among Normal and Sickle Cell Adults Is Not Related to Nucleotide Substitutions in the Gamma Promoter Regions

    Variation in Hemoglobin F Production Among Normal and Sickle Cell Adults Is Not Related to Nucleotide Substitutions in the Gamma Promoter Regions by Economou, E.P., Antonarakis, S.E., Kazazian, H.H., Serjeant, G.R., Dover, G.J.

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  6. 6
    5-Azacytidine Increases HbF Production and Reduces Anemia in Sickle Cell Disease: Dose-Response Analysis of Subcutaneous and Oral Dosage Regimens

    5-Azacytidine Increases HbF Production and Reduces Anemia in Sickle Cell Disease: Dose-Response Analysis of Subcutaneous and Oral Dosage Regimens by Dover, G.J., Charache, S., Boyer, S.H., Vogelsang, G., Moyer, M.

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  7. 7
    Fetal Hemoglobin-Containing Cells Have the Same Mean Corpuscular Hemoglobin as Cells Without Fetal Hemoglobin: A Reciprocal Relationship Between Gamma- and Beta-Globin Gene Expression in Normal Subjects and in Those With High Fetal Hemoglobin Production

    Fetal Hemoglobin-Containing Cells Have the Same Mean Corpuscular Hemoglobin as Cells Without Fetal Hemoglobin: A Reciprocal Relationship Between Gamma- and Beta-Globin Gene Express... by Dover, G.J., Boyer, S.H.

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  8. 8
    The Cellular Basis for Different Fetal Hemoglobin Levels Among Sickle Cell Individuals With Two, Three, and Four Alpha-Globin Genes

    The Cellular Basis for Different Fetal Hemoglobin Levels Among Sickle Cell Individuals With Two, Three, and Four Alpha-Globin Genes by Dover, G.J., Chang, V.T., Boyer, S.H., Serjeant, G.R., Antonarakis, S., Higgs, D.R.

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  9. 9
    Results of the centralisation of adult emergency oral and maxillofacial surgical services at the University Hospital, Birmingham

    Results of the centralisation of adult emergency oral and maxillofacial surgical services at the University Hospital, Birmingham by James, G.J., Gibbons, A.J., Srinivasan, D., Dover, M. Stephen

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  10. 10
    On the defect structure of grain boundaries in Ba2YCu3O7–x

    On the defect structure of grain boundaries in Ba2YCu3O7–x by Nakahara, S., Fisanick, G.J., Yan, M.F., Van Dover, R.B., Boone, T., Moore, R.

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  11. 11
    On the defect structure of grain boundaries in Ba 2YCu 3O 7– x

    On the defect structure of grain boundaries in Ba 2YCu 3O 7– x by Nakahara, S., Fisanick, G.J., Yan, M.F., Van Dover, R.B., Boone, T., Moore, R.

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