Search Results - Derclaye, Isabelle

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  1. 1
    Haemoglobin Ottawa, sickle cell trait and vaso‐occlusive crises

    Haemoglobin Ottawa, sickle cell trait and vaso‐occlusive crises by Bobillier, Cécile, Derclaye, Isabelle, Ferrant, Augustin, Maisin, Diane

    Published in EJHaem
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  2. 2
    Detection of hemoglobin Kinshasa by a capillary electrophoresis method

    Detection of hemoglobin Kinshasa by a capillary electrophoresis method by Deltombe, Matthieu, Benamour, Meryem, Derclaye, Isabelle, Maisin, Diane

    Published in Clinica chimica acta
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  3. 3
    Validation of a recombinant DNA construct (μlLCR and full-length β-globin gene) for quantification of human β-globin expression: Application to mutations in the promoter, intronic, and 5'- and 3'-untranslated regions of the human β-globin gene

    Validation of a recombinant DNA construct (μlLCR and full-length β-globin gene) for quantification of human β-globin expression: Application to mutations in the promoter, intronic,... by IRENGE, Leonid M, HEUSTERSPREUTE, Michel, PHILIYPE, Marianne, DERCLAVE, Isabelle, ROBERT, Annie, GALA, Jean-Luc

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  4. 4
    Severe hereditary haemolytic anaemia in a Caucasian newborn: a new fetal haemoglobin variant Hb F-Bonheiden ((G)gamma 38(C4) Thr-->Pro)

    Severe hereditary haemolytic anaemia in a Caucasian newborn: a new fetal haemoglobin variant Hb F-Bonheiden ((G)gamma 38(C4) Thr-->Pro) by Van den Driessche, Marleen, Moerman, Jan, Moens, Marc, Van Eldere, Stefaan, Derclaye, Isabelle, Philippe, Marianne

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  5. 5
    Severe hereditary haemolytic anaemia in a Caucasian newborn: a new fetal haemoglobin variant Hb F-Bonheiden (Gγ 38(C4) Thr → Pro)

    Severe hereditary haemolytic anaemia in a Caucasian newborn: a new fetal haemoglobin variant Hb F-Bonheiden (Gγ 38(C4) Thr → Pro) by VAN DEN DRIESSCHE, Marleen, MOERMAN, Jan, MOENS, Marc, VAN ELDERE, Stefaan, DERCLAYE, Isabelle, PHILIPPE, Marianne

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  6. 6
    Beta-thalassaemia in indigenous Belgian families : identification of a novel mutation

    Beta-thalassaemia in indigenous Belgian families : identification of a novel mutation by HEUSTERPREUTE, M, DERCLAYE, I, GALA, J.-L, VAN GEET, C, FERRANT, A, MALCHAIRE, Y, THONNARD, J, VAERMAN, J.-L, PHILIPPE, M

    Published in Human genetics
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