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Items where Author is "White, SM"

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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.
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