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Items where Author is "White, SM"
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Number of items: 4.
Jayasinghe, K, Stark, Z, Kerr, PG, Gaff, C, Martyn, M, Whitlam, J, Creighton, B, Donaldson, E, Hunter, M, Jarmolowicz, A, Johnstone, L, Krzesinski, E, Lunke, S, Lynch, E, Nicholls, K, Patel, C, Prawer, Y, Ryan, J, See, EJ, Talbot, A, Trainer, A, Tytherleigh, R, Valente, G, Wallis, M ORCID: 0000-0002-5441-1732, Wardrop, L, West, KH, White, SM, Wilkins, E, Mallett, AJ and Quinlan, C 2021
, 'Clinical impact of genomic testing in patients with suspected monogenic kidney disease'
, Genetics in Medicine, vol. 23, no. 1
, pp. 183-191
, doi: https://doi.org/10.1038/s41436-020-00963-4.
Jayasinghe, K, Stark, Z, Kerr, PG, Gaff, C, Martyn, M, Whitlam, J, Creighton, B, Donaldson, E, Hunter, M, Jarmolowicz, A, Johnstone, L, Krzesinski, E, Lunke, S, Lynch, E, Nicholls, K, Patel, C, Prawer, Y, Ryan, J, See, EJ, Talbot, A, Trainer, A, Tytherleigh, R, Valente, G, Wallis, M, Wardrop, L, West, KH, White, SM, Wilkins, E, Mallett, AJ and Quinlan, C 2020
, 'Clinical impact of genomic testing in patients with suspected monogenic kidney disease'
, Genetics in Medicine
, pp. 1-9
, doi: https://doi.org/10.1038/s41436-020-00963-4.
Rafehi, H, Szmulewicz, DJ, Pope, K, Wallis, M, Christodoulou, J, White, SM, Delatycki, MB, Lockhart, PJ and Bahlo, M 2020
, 'Rapid diagnosis of spinocerebellar ataxia 36 in a three-generation family using short-read whole-genome sequencing data'
, Movement Disorders
, pp. 1-6
, doi: https://doi.org/10.1002/mds.28105.
Sachdev, R, Field, M, Baynam, GS, Beilby, J, Berarducci, M, Berman, Y, Boughtwood, T, Cusack, MB, Fitzgerald, V, Fletcher, J, Freckmann, ML, Grainger, N, Kirk, E, Lundie, B, Lunke, S, McGregor, L, Mowat, D, Parasivam, G, Tyrell, V, Wallis, M ORCID: 0000-0002-5441-1732, White, SM and S L Ma, A 2021
, 'Paediatric genomic testing: Navigating medicare rebatable genomic testing'
, Journal of Paediatrics and Child Health, vol. 57, no. 4
, pp. 477-483
, doi: https://doi.org/10.1111/jpc.15382.
This list was generated on Thu Jun 1 01:54:25 2023 AEST.