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Exploring the benefits, harms, and costs of genomic newborn screening for rare diseases by Baple, EL, Scott, RH, Banka, S, Buchanan, J, Fish, L, Wynn, S, Wilkinson, J, Ellard, S, MacArthur, DG, Stark, Z
Published 2024Journal article -
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Genomic diagnosis and care co-ordination for monogenic inflammatory bowel disease in children and adults: consensus guideline on behalf of the British Society of Gastroenterology a... by Kammermeier, J, Lamb, CA, Jones, KDJ, Anderson, CA, Baple, EL, Bolton, C, Braggins, H, Coulter, TI, Gilmour, KC, Gregory, V, Hambleton, S, Hartley, D, Hawthorne, AB, Hearn, S, Laurence, A, Parkes, M, Russell, RK, Speight, RA, Travis, S, Wilson, DC, Uhlig, HH
Published 2023Journal article -
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‘Something that helped the whole picture’: Experiences of parents offered rapid prenatal exome sequencing in routine clinical care in the English National Health Service by McInnes‐Dean, H, Mellis, R, Daniel, M, Walton, H, Baple, EL, Bertoli, M, Fisher, J, Gajewska‐Knapik, K, Holder‐Espinasse, M, Lafarge, C, Leeson‐Beevers, K, McEwan, A, Pandya, P, Parker, M, Peet, S, Roberts, L, Sankaran, S, Smith, A, Tapon, D, Wu, WH, Wynn, SL, Chitty, LS, Hill, M, Peter, M
Published 2024Journal article