Search Results - Jennens, M.

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  1. 1
    A molecular tool to assess the pathological relevance of alpha-globin DNA variants

    A molecular tool to assess the pathological relevance of alpha-globin DNA variants by Qadah, T., Finlayson, J., Newbound, C., Pell, N., Jennens, M., Holmes, P., Grey, D., Beilby, J., Ghassemifar, Reza

    Published 2012
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  2. 2
    a-Thalassemia trait caused by frameshift mutations in exon 2 of the a2-globin gene: HBA2:c.131delT and HBA2:c.143delA

    a-Thalassemia trait caused by frameshift mutations in exon 2 of the a2-globin gene: HBA2:c.131delT and HBA2:c.143delA by Finlayson, J., Ghassemifar, Reza, Holmes, P., Grey, D., Newbound, C., Pell, N., Jennens, M., Greenwood, L., Beilby, J.

    Published 2012
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  3. 3
    Hb lynwood [a107(G14) (-T) (a2) HBA2:c.323delT)] in conjunction with the a3.7 deletion produces a moderately severe a-thalassemia phenotype

    Hb lynwood [a107(G14) (-T) (a2) HBA2:c.323delT)] in conjunction with the a3.7 deletion produces a moderately severe a-thalassemia phenotype by Finlayson, J., Ghassemifar, Reza, Holmes, P., Grey, D., Newbound, C., Pell, N., Jennens, M., MacAulay, C., Greenwood, L., Beilby, J.

    Published 2011
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  4. 4
    Hb East Timor [ß80(EF4)Asn?His, AAC>CAC (HBB c.241A>C)], a variant hemoglobin associated with normal hematology

    Hb East Timor [ß80(EF4)Asn?His, AAC>CAC (HBB c.241A>C)], a variant hemoglobin associated with normal hematology by Finlayson, J., Ghassemifar, Reza, Holmes, P., Grey, D., Figliomeni, L., Newbound, C., Pell, N., Kersten, M., Jennens, M., Macaulay, C., Greenwood, L., Beilby, J.

    Published 2010
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