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Items where Author is "Delatycki, MB"
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Number of items: 5.
Crombie, DE, Curl, CL, Raaijmakers, AJ, Sivakumaran, P, Kulkarni, T, Wong, RCB, Minami, I, Evans-Galea, MV, Lim, SY, Delbridge, L, Corben, LA, Dottori, M, Nakatsuji, N, Trounce, IA, Hewitt, AW 
ORCID: 0000-0002-5123-5999, Delatycki, MB, Pera, MF and Pebay, A 2017
, 'Friedreich's ataxia induced pluripotent stem cell-derived cardiomyocytes display electrophysiological abnormalities and calcium handling deficiency'
, Aging, vol. 9, no. 5
, pp. 1440-1452
, doi: https://doi.org/10.18632/aging.101247.
ORCID: 0000-0002-5123-5999, Delatycki, MB, Pera, MF and Pebay, A 2017
, 'Friedreich's ataxia induced pluripotent stem cell-derived cardiomyocytes display electrophysiological abnormalities and calcium handling deficiency'
, Aging, vol. 9, no. 5
, pp. 1440-1452
, doi: https://doi.org/10.18632/aging.101247.
Eratne, D, Schneider, A, Lynch, E, Martyn, M, Velakoulis, D, Fahey, M, Kwan, P, Leventer, R, Rafehi, H, Chong, B, Stark, Z, Lunke, S, Phelan, DG, O'Keefe, M, Siemering, K, West, K, Sexton, A, Jarmolowicz, A, Taylor, JA, Schultz, J, Purvis, R, Uebergang, E, Chalinor, H, Creighton, B, Gelfand, N, Saks, T, Prawer, Y, Smagarinsky, Y, Pan, T, Goranitis, I, Ademi, Z, Gaff, C, Huq, A, Walsh, M, James, PA, Krzesinski, EI, Wallis, M ORCID: 0000-0002-5441-1732, Stutterd, CA, Bahlo, M, Delatycki, MB and Berkovic, SF 2021
, 'The clinical utility of exome sequencing and extended bioinformatic analyses in adolescents and adults with a broad range of neurological phenotypes: an Australian perspective'
, Journal of the Neurological Sciences, vol. 420
, doi: https://doi.org/10.1016/j.jns.2020.117260.
ORCID: 0000-0002-5441-1732, Stutterd, CA, Bahlo, M, Delatycki, MB and Berkovic, SF 2021
, 'The clinical utility of exome sequencing and extended bioinformatic analyses in adolescents and adults with a broad range of neurological phenotypes: an Australian perspective'
, Journal of the Neurological Sciences, vol. 420
, doi: https://doi.org/10.1016/j.jns.2020.117260.
Eratne, D, Schneider, A, Lynch, E, Martyn, M, Velakoulis, D, Fahey, M, Kwan, P, Leventer, R, Rafehi, H, Chong, B, Stark, Z, Lunke, S, Phelan, DG, O'Keefe, M, Siemering, K, West, K, Sexton, A, Jarmolowicz, A, Taylor, JA, Schultz, J, Purvis, R, Uebergang, E, Chalinor, H, Creighton, B, Gelfand, N, Saks, T, Prawer, Y, Smagarinsky, Y, Pan, T, Goranitis, I, Ademi, Z, Gaff, C, Huq, A, Walsh, M, James, PA, Krzesinski, EI, Wallis, M ORCID: 0000-0002-5441-1732, Stutterd, CA, Bahlo, M, Delatycki, MB and Berkovic, SF 2021
, 'The clinical utility of exome sequencing and extended bioinformatic analyses in adolescents and adults with a broad range of neurological phenotypes: an Australian perspective'
, Journal of the Neurological Sciences, vol. 420
, doi: https://doi.org/10.1016/j.jns.2020.117260.
ORCID: 0000-0002-5441-1732, Stutterd, CA, Bahlo, M, Delatycki, MB and Berkovic, SF 2021
, 'The clinical utility of exome sequencing and extended bioinformatic analyses in adolescents and adults with a broad range of neurological phenotypes: an Australian perspective'
, Journal of the Neurological Sciences, vol. 420
, doi: https://doi.org/10.1016/j.jns.2020.117260.
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.
Tiller, J, Morris, S, Rice, T, Barter, K, Riaz, M, Keogh, L, Delatycki, MB, Otlowsk, M ORCID: 0000-0003-4707-4325 and Lacaze, P 2019
, 'Genetic discrimination by Australian insurance companies: a survey of consumer experiences'
, European Journal of Human Genetics
, pp. 1-6
, doi: https://doi.org/10.1038/s41431-019-0426-1.
ORCID: 0000-0003-4707-4325 and Lacaze, P 2019
, 'Genetic discrimination by Australian insurance companies: a survey of consumer experiences'
, European Journal of Human Genetics
, pp. 1-6
, doi: https://doi.org/10.1038/s41431-019-0426-1.