A. Dixon-Mciver

发表

Screening for anaplastic lymphoma kinase (ALK) gene rearrangements in non‐small‐cell lung cancer in New Zealand

S. Tin Tin, M. Elwood, D. Love, 2020, Internal medicine journal.

Assessing copy number abnormalities and copy-neutral loss-of-heterozygosity across the genome as best practice in diagnostic evaluation of acute myeloid leukemia: An evidence-based review from the cancer genomics consortium (CGC) myeloid neoplasms working group.

M. Slovak, F. Quintero-Rivera, G. Raca, 2018, Cancer genetics.

NRASQ61R Mutation-specific Immunohistochemistry is Highly Specific for Either NRASQ61R or KRASQ61R Mutation in Colorectal Carcinoma

C. Toon, A. Gill, J. Andrici, 2017, Applied immunohistochemistry & molecular morphology : AIMM.

Assessing copy number aberrations and copy neutral loss of heterozygosity across the genome as best practice: An evidence based review of clinical utility from the cancer genomics consortium (CGC) working group for myelodysplastic syndrome, myelodysplastic/myeloproliferative and myeloproliferative n

M. Slovak, F. Quintero-Rivera, G. Raca, 2018, Cancer genetics.

Myelodysplastic syndrome associated with trisomy 2.

D. Provan, J. Amess, A. Dixon-Mciver, 2005, Clinical and laboratory haematology.

Mutations of CEBPA in acute myeloid leukemia FAB types M1 and M2

T. Lister, A. Rohatiner, J. Fitzgibbon, 2003, Genes, chromosomes & cancer.

MicroRNA detection in bone marrow cells by LNA-FISH.

S. Debernardi, A. Dixon-Mciver, 2010, Methods in molecular biology.

Distinctive Patterns of MicroRNA Expression Associated with Karyotype in Acute Myeloid Leukaemia

Jean-Baptiste Cazier, Bryan D. Young, Charles A. Mein, 2008, PloS one.

MicroRNA miR-181a correlates with morphological sub-class of acute myeloid leukaemia and the expression of its target genes in global genome-wide analysis

T Chaplin, B D Young, B. Young, 2007, Leukemia.

ATR16 Syndrome: Mechanisms Linking Monosomy to Phenotype

A. Wilkie, D. Higgs, J. Traeger-Synodinos, 2019, bioRxiv.

Emerging technologies in paediatric leukaemia.

A. Dixon-Mciver, 2015, Translational pediatrics.

Detection of complex genomic signatures associated with risk in plasma cell disorders.

R. Scott, A. Enjeti, P. Rowlings, 2017, Cancer genetics.

Assessing copy number abnormalities and copy-neutral loss-of-heterozygosity across the genome as best practice in diagnostic evaluation of acute myeloid leukemia: An evidence-based review from the cancer genomics consortium (CGC) myeloid neoplasms working group.

M. Slovak, F. Quintero-Rivera, G. Raca, 2018, Cancer genetics.

ATR-16 syndrome: mechanisms linking monosomy to phenotype

A. Wilkie, D. Higgs, J. Traeger-Synodinos, 2020, Journal of Medical Genetics.