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Methods in Molecular Biology (Clifton, N.J.)|December 3, 2016
Recurrent Cytogenetic Abnormalities in Myelodysplastic SyndromesMeaghan Wall
European Journal of Haematology|May 22, 2015
The molecular pathogenesis of B-cell non-Hodgkin lymphomaPiers A Blombery, Meaghan Wall, John F Seymour
Molecular Cytogenetics|December 15, 2020
Detailed molecular cytogenetic characterisation of the myeloid cell line U937 reveals the fate of homologous chromosomes and shows that centromere capture is a feature of genome instabilityRuth N MacKinnon, Joanne Peverall, Lynda J Campbell, et al.
Cancer Genetics|May 4, 2011
A cryptic deletion in 5q31.2 provides further evidence for a minimally deleted region in myelodysplastic syndromesRuth N MacKinnon, George Kannourakis, Meaghan Wall, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics|January 14, 2021
Newborn bloodspot screening in the time of COVID-19Ronda F Greaves, James Pitt, Candice McGregor, et al.
Cytogenetic and Genome Research|March 6, 2017
The Dicentric Chromosome dic(20;22) Is a Recurrent Abnormality in Myelodysplastic Syndromes and Is a Product of Telomere FusionRuth N MacKinnon, Hendrika M Duivenvoorden, Lynda J Campbell, et al.
Pharmacogenomics and Personalized Medicine|July 7, 2023
Are We Ready for Whole Population Genomic Sequencing of Asymptomatic Newborns?Danya F Vears, Julian Savulescu, John Christodoulou, et al.
Therapeutic Advances in Hematology|February 3, 2016
Current challenges and novel treatment strategies in double hit lymphomasMary Ann Anderson, Alpha Tsui, Meaghan Wall, et al.
Molecular Cytogenetics|February 4, 2012
CGH and SNP array using DNA extracted from fixed cytogenetic preparations and long-term refrigerated bone marrow specimensRuth N Mackinnon, Carly Selan, Adrian Zordan, et al.
Genes, Chromosomes & Cancer|July 21, 2010
The paradox of 20q11.21 amplification in a subset of cases of myeloid malignancy with chromosome 20 deletionRuth N Mackinnon, Carly Selan, Meaghan Wall, et al.
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