Результати пошуку - Gavin Ryan

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  1. 1
    Germline heterozygous DDX41 variants in a subset of familial myelodysplasia and acute myeloid leukemia

    Germline heterozygous DDX41 variants in a subset of familial myelodysplasia and acute myeloid leukemia за авторством Shirleny Cardoso, Gavin Ryan, Amanda J. Walne, Alicia Ellison, Robert Lowe, Hemanth Tummala, Ana Rio‐Machín, Laura C. Collopy, Ahad Al Seraihi, Yvonne Wallis, Paula Page, Susanna Akiki, Jude Fitzgibbon, Tom Vulliamy, Inderjeet Dokal

    Опубліковано 2016
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    Carta
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  2. 2
    The impact of inversions across 33,924 families with rare disease from a national genome sequencing project

    The impact of inversions across 33,924 families with rare disease from a national genome sequencing project за авторством Alistair T. Pagnamenta, Jing Yu, Susan Walker, Alexandra Noble, Jenny Lord, Prasun Dutta, Mona Hashim, Carlos Camps, Hannah Green, Smrithi Devaiah, Lina Nashef, Jason Parr, Carl Fratter, Rana Hussein, Sarah Lindsay, Fiona Lalloo, Benito Banos‐Pinero, David M. Evans, Lucy Mallin, Adrian J. Waite, Julie Evans, Andrew G. Newman, Zoe Allen, Cristina Perez‐Becerril, Gavin Ryan, Rachel Hart, John‐Stephen Taylor, Tina Bedenham, Emma Clement, Ed Blair, Eleanor Hay, Francesca Forzano, Jenny Higgs, Natalie Canham, Anirban Majumdar, Meriel McEntagart, Nayana Lahiri, Helen Stewart, Sarah Smithson, Eduardo Calpena, Adam Jackson, Siddharth Banka, Hannah Titheradge, Ruth McGowan, Julia Rankin, Charles Shaw‐Smith, D. Gareth Evans, George J. Burghel, Miriam J. Smith, Emily E. Anderson, Rajesh Madhu, Helen V. Firth, Sian Ellard, Paul Brennan, Claire Anderson, Doug Taupin, Mark T. Rogers, Jackie A. Cook, Miranda Durkie, James E. East, Darren Fowler, Louise C. Wilson, Rebecca Igbokwe, Alice Gardham, Ian Tomlinson, Diana Baralle, Holm H. Uhlig, Jenny C. Taylor

    Опубліковано 2024
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    Artigo
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