M. Dainton

发表

PLATINUM AGENTS AND SECONDARY MYELOID LEUKAEMIA: TWO CASES TREATED ONLY WITH PLATINUM‐BASED DRUGS

M. Gore, D. Catovsky, T. Min, 1996, British journal of haematology.

Angiomatoid fibrous histiocytoma: comparison of fluorescence in situ hybridization and reverse transcription polymerase chain reaction as adjunct diagnostic modalities.

C. Fisher, K. Thway, J. Swansbury, 2015, Annals of diagnostic pathology.

The comparative utility of fluorescence in situ hybridization and reverse transcription-polymerase chain reaction in the diagnosis of alveolar rhabdomyosarcoma

C. Fisher, K. Thway, J. Swansbury, 2015, Virchows Archiv.

Lung adenocarcinoma with concurrent exon 19 EGFR mutation and ALK rearrangement responding to erlotinib.

A. Nicholson, A. Wotherspoon, M. O'Brien, 2011, Journal of thoracic oncology : official publication of the International Association for the Study of Lung Cancer.

Peripheral blood stem cells used to augment autologous bone marrow transplantation.

C. R. Pinkerton, V. Shepherd, M. Dainton, 1994, Archives of disease in childhood.

Transplantation of autologous peripheral blood stem cells mobilized using GM-CSF for acute leukemia with myelofibrosis.

J. Mehta, J. Treleaven, R. Powles, 1993, Leukemia & lymphoma.

Haploinsufficiency of the MLL and TOB2 genes in lymphoid malignancy

C. Harrison, J. Strefford, Z. Konn, 2010, Leukemia.

Acute myelomonocytic leukemia with t(10;11)(p13;q23): Heterogeneity of breakpoints at 11q23 and association with recombinase activation

M. Dyer, L. Kearney, D. Catovsky, 1994, Genes, chromosomes & cancer.

Fluorescence in situ hybridization analysis of t(3; 12)(q26; p13): a recurring chromosomal abnormality involving the TEL gene (ETV6) in myelodysplastic syndromes.

P. Marynen, J. Grosgeorge, S. Raynaud, 1996, Blood.

Fluorescence In Situ Hybridization Analysis of t ( 3 ; 12 ) ( q 26 ; p 13 ) : A Recurring Chromosomal Abnormality Involving the TEL Gene ( E T V 6 ) in Myelodysplastic Syndromes

C. Reid, B. Taillan, Dyer, 2022 .

Incidence of MLL Rearrangement in Acute Myeloid Leukemia, and a CALM - AF10 Fusion in M4 Type Acute Myeloblastic Leukemia

D. Catovsky, D. Jadayel, S. Abdou, 2002, Leukemia & lymphoma.

Monosomy X as the sole cytogenetic abnormality in acute lymphoblastic leukemia: a report of two new patients.

J. Bueno, G. Swansbury, J. Treleaven, 1999, Leukemia & lymphoma.

myelodysplastic syndromes in recurring chromosomal abnormality involving the TEL gene (ETV6) Fluorescence in situ hybridization analysis of t(3; 12)(q26; p13): a

P. Marynen, J. Grosgeorge, N. Ayraud, 2011 .

ALK-positive inflammatory myofibroblastic tumor harboring ALK gene rearrangement, occurring after allogeneic stem cell transplant in an adult male.

C. Fisher, I. Judson, K. Thway, 2016, Pathology, research and practice.

Additional chromosome abnormalities confer worse prognosis in acute promyelocytic leukaemia

J. Mehta, D. Catovsky, L. Hiorns, 1997, British journal of haematology.

Disease Features in Acute Myeloid Leukemia with t(8;21)(q22;q22). Influence of Age, Secondary Karyotype Abnormalities, CD19 Status, and Extramedullar Leukemia on Survival

D. Catovsky, E. Matutes, M. Durosinmi, 2000, Leukemia & lymphoma.

ALK translocation is associated with ALK immunoreactivity and extensive signet-ring morphology in primary lung adenocarcinoma.

A. Nicholson, J. Swansbury, S. Popat, 2012, Lung cancer.