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Items where Author is "Wallis, M"

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Number of items: 5.

Article

Brailsford, G, Cash, E, Burke, J, Kirkland, G, Wallis, M, Mallett, A and Jose, MD ORCID: 0000-0002-9589-0071 2020 , 'Genetic kidney disease in Southern Tasmania' , Kidney international reports, vol. 5, no. 4 , pp. 534-537 , doi: 10.1016/j.ekir.2020.01.015.

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: 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: 10.1002/mds.28105.

Wallis, M, Pope-Couston, R, Mansour, J, Amor, DJ, Tang, P and Stock-Myer, S 2020 , 'Lymphedema distichiasis syndrome may be caused by FOXC2 promoter-enhancer dissociation and disruption of a topological associated domain' , American Journal of Medical Genetics. Part A , pp. 1-7 , doi: 10.1002/ajmg.a.61935.

Zhang, T, Wallis, M, Petrovic, V, Challis, J, Kalitsis, P and Hudson, DF 2019 , 'Loss of TOP3B leads to increased R-loop formation and genome instability' , Open Biology, vol. 9, no. 12 , pp. 1-15 , doi: 10.1098/rsob.190222.

This list was generated on Fri May 14 01:59:48 2021 AEST.
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