Hasil Pencarian - Shona Handisides

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  1. 1
    Case report: tuberous sclerosis and persistent hyperplastic primary vitreous

    Case report: tuberous sclerosis and persistent hyperplastic primary vitreous oleh Hayley Wong, Sarah Bowie, Shona Handisides, Julia Escardó-Paton

    Diterbitkan 2022-07-01
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  2. 2
    Whole Exome Sequencing Reveals Compound Heterozygosity for Ethnically Distinct PEX7 Mutations Responsible for Rhizomelic Chondrodysplasia Punctata, Type 1

    Whole Exome Sequencing Reveals Compound Heterozygosity for Ethnically Distinct PEX7 Mutations Responsible for Rhizomelic Chondrodysplasia Punctata, Type 1 oleh Jessie C. Jacobsen, Emma Glamuzina, Juliet Taylor, Brendan Swan, Shona Handisides, Callum Wilson, Michael Fietz, Tessa van Dijk, Bart Appelhof, Rosamund Hill, Rosemary Marks, Donald R. Love, Stephen P. Robertson, Russell G. Snell, Klaus Lehnert

    Diterbitkan 2015-01-01
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