Resultados de procura - Christopher Thornborough

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  1. 1
    Combined Mutation Screening of NKX2-5, GATA4, and TBX5 in Congenital Heart Disease: Multiple Heterozygosity and Novel Mutations

    Combined Mutation Screening of NKX2-5, GATA4, and TBX5 in Congenital Heart Disease: Multiple Heterozygosity and Novel Mutations por Javier T Granados-Riveron, Mark Pope, Frances Bu’Lock, Christopher Thornborough, Jacqueline Eason, Kerry Setchfield, Ami Ketley, Edwin P. Kirk, Diane Fatkin, Michael P. Feneley, Richard P. Harvey, J. David Brook

    Publicado 2011
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  2. 2
    α-Cardiac myosin heavy chain (MYH6) mutations affecting myofibril formation are associated with congenital heart defects

    α-Cardiac myosin heavy chain (MYH6) mutations affecting myofibril formation are associated with congenital heart defects por Javier T Granados-Riveron, Tushar K. Ghosh, Mark Pope, Frances Bu’Lock, Christopher Thornborough, Jacqueline Eason, Edwin P. Kirk, Diane Fatkin, Michael P. Feneley, Richard P. Harvey, John A.L. Armour, J. David Brook

    Publicado 2010
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  3. 3
    Tropomyosin 1: Multiple roles in the developing heart and in the formation of congenital heart defects

    Tropomyosin 1: Multiple roles in the developing heart and in the formation of congenital heart defects por Jennifer England, Javier T Granados-Riveron, Luis Polo‐Parada, Diji Kuriakose, Chris Moore, J. David Brook, Catrin S. Rutland, Kerry Setchfield, Chris Gell, Tushar K. Ghosh, Frances Bu’Lock, Christopher Thornborough, Elisabeth Ehler, Siobhan Loughna

    Publicado 2017
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