Search Results - Elyas, Basil

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  1. 1
    Microduplication and Triplication of 22q11.2: A Highly Variable Syndrome

    Microduplication and Triplication of 22q11.2: A Highly Variable Syndrome by Yobb, Twila M., Somerville, Martin J., Willatt, Lionel, Firth, Helen V., Harrison, Karen, MacKenzie, Jennifer, Gallo, Natasha, Morrow, Bernice E., Shaffer, Lisa G., Babcock, Melanie, Chernos, Judy, Bernier, Francois, Sprysak, Kathy, Christiansen, Jesse, Haase, Shelagh, Elyas, Basil, Lilley, Margaret, Bamforth, Steven, McDermid, Heather E.

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  2. 2
    Chromosome 1q21.1 Contiguous Gene Deletion Is Associated With Congenital Heart Disease

    Chromosome 1q21.1 Contiguous Gene Deletion Is Associated With Congenital Heart Disease by Christiansen, Jesse, Dyck, John D, Elyas, Basil G, Lilley, Margaret, Bamforth, J Stephen, Hicks, Mark, Sprysak, Kathleen A, Tomaszewski, Robert, Haase, Shelagh M, Vicen-Wyhony, Leanne M, Somerville, Martin J

    Published in Circulation research
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  3. 3
    Integration of combined heteroduplex/restriction fragment length polymorphism analysis on an electrophoresis microchip for the detection of hereditary haemochromatosis

    Integration of combined heteroduplex/restriction fragment length polymorphism analysis on an electrophoresis microchip for the detection of hereditary haemochromatosis by FOOTZ, Tim, SOMERVILLE, Martin J, TOMASZEWSKI, Robert, ELYAS, Basil, BACKHOUSE, Christopher J

    Published in Analyst (London)
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  4. 4
    An HFE Intronic Variant Promotes Misdiagnosis of Hereditary Hemochromatosis

    An HFE Intronic Variant Promotes Misdiagnosis of Hereditary Hemochromatosis by Somerville, Martin J., Sprysak, Kathleen A., Hicks, Mark, Elyas, Basil G., Vicen-Wyhony, Leanne

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