M. Martineau

发表

Interphase molecular cytogenetic screening for chromosomal abnormalities of prognostic significance in childhood acute lymphoblastic leukaemia: a UK Cancer Cytogenetics Group Study

F. Ross, C. Harrison, A. Moorman, 2005, British journal of haematology.

Amplification of AML1 on a duplicated chromosome 21 in acute lymphoblastic leukemia: a study of 20 cases

C. Harrison, A. Moorman, H. Robinson, 2003, Leukemia.

A unique variant of ETV6/AML1 fusion in a child with acute lymphoblastic leukemia

M. Greaves, C. Harrison, A. Ford, 2003, Leukemia.

Amplification of AML1 in acute lymphoblastic leukemia is associated with a poor outcome

S. Richards, C. Harrison, A. Moorman, 2003, Leukemia.

A Fluorescence in Situ Hybridization Map of 6q Deletions in Acute Lymphocytic Leukemia

L. Foroni, C. Harrison, P. Sinclair, 2004, Cancer Research.

Complex chromosomal abnormalities in utero, 5 years before leukaemia *

Z. Zemanová, K. Michalová, C. Harrison, 2004, British journal of haematology.

A Fluorescence in Situ Hybridization Map of 6q Deletions in Acute Lymphocytic Leukemia: Identification and Analysis of a Candidate Tumor Suppressor Gene

L. Foroni, C. Harrison, P. Sinclair, 2004 .

A Fluorescence in Situ Hybridization Map of 6 q Deletions in Acute Lymphocytic Leukemia : Identification and Analysis of a Candidate Tumor Suppressor Gene

L. Foroni, C. Harrison, P. Sinclair, 2004 .

Three further cases of t(8;14)(q11.2;q32) in acute lymphoblastic leukemia

M. Humphreys, L. Harewood, C. Harrison, 2001, Leukemia.

Disruption of ETV6 in intron 2 results in upregulatory and insertional events in childhood acute lymphoblastic leukaemia

C. Harrison, J. Strefford, Z. Konn, 2008, Leukemia.

Derivative chromosome 9 deletions are a significant feature of childhood Philadelphia chromosome positive acute lymphoblastic leukaemia

C. Harrison, A. Moorman, J. Strefford, 2005, Leukemia.

Haploinsufficiency of the MLL and TOB2 genes in lymphoid malignancy

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

Cytogenetics of long‐term survivors of ETV6‐RUNX1 fusion positive acute lymphoblastic leukemia

S. Richards, C. Harrison, J. Swansbury, 2009, Genes, chromosomes & cancer.

ETV6/RUNX1 fusion at diagnosis and relapse: Some prognostic indications

S. Richards, F. Ross, C. Harrison, 2005, Genes, chromosomes & cancer.

Is trisomy 5 a distinct cytogenetic subgroup in acute lymphoblastic leukemia?

C. Harrison, A. Moorman, M. Martineau, 2004, Cancer genetics and cytogenetics.

No chromosome arm unturned: in memory of Roland Berger 1934–2012

A. Hagemeijer, O. Bernard, H. Berghe, 2014, Leukemia.

Amplification of the ABL gene in T-cell acute lymphoblastic leukemia

E. Cameron, C. Harrison, A. Moorman, 2004, Leukemia.

Monosomy 20 as a pointer to dicentric (9;20) in acute lymphoblastic leukemia

O. Eden, A. Moorman, A. Goldstone, 2000, Leukemia.

Probes for hidden hyperdiploidy in acute lymphoblastic leukaemia

A. Moorman, M. Martineau, L. Secker-Walker, 1996, Genes, chromosomes & cancer.

Chromosomes in human testicular tumours

M. Martineau, 1969, The Journal of pathology.

M. Martineau, 1966, Lancet.

ETV6/AML1 fusion by FISH in adult acute lymphoblastic leukemia

H. Prentice, A. Goldstone, L. Harewood, 2002, Leukemia.

A diminutive chromosome 21 centromere in acute lymphoblastic leukemia.

C. Harrison, L. Harewood, Z. J. Broadfield, 2006, Cancer genetics and cytogenetics.

Short communication A diminutive chromosome 21 centromere in acute lymphoblastic leukemia

C. Harrison, L. Harewood, M. Martineau, 2006 .

Isochromosomes in acute lymphoblastic leukaemia: I(21q) is a significant finding

A. Moorman, M. Martineau, L. Secker-Walker, 1996, Genes, chromosomes & cancer.

Molecular cytogenetic characterization of TCF3 (E2A)/19p13.3 rearrangements in B‐cell precursor acute lymphoblastic leukemia

Anthony V Moorman, C. Harrison, A. Moorman, 2007, Genes, chromosomes & cancer.

The Leukaemia Research Fund/United Kingdom Cancer Cytogenetics Group Karyotype Database in acute lymphoblastic leukaemia: a valuable resource for patient management

M. Martineau, L. Secker-Walker, C. J. Harrison, 2001, British journal of haematology.

Three distinct subgroups of hypodiploidy in acute lymphoblastic leukaemia

S. Richards, A. Vora, A. Moorman, 2004, British journal of haematology.

Association of 17p loss with late-stage or refractory disease in hematologic malignancy.

H. Prentice, A. Mehta, A. Moorman, 1994, Cancer genetics and cytogenetics.

Demonstration of acquired hemizygosity and clonality in acute lymphoblastic leukemia with chromosome 7 abnormalities using hypervariable DNA probes

M. Martineau, L. Secker-Walker, C. Shippey, 1990, Genes, chromosomes & cancer.

Outcome heterogeneity in childhood high-hyperdiploid acute lymphoblastic leukemia.

S. Richards, C. Harrison, A. Moorman, 2003, Blood.

Karyotype is an independent prognostic factor in adult acute lymphoblastic leukemia (ALL): analysis of cytogenetic data from patients treated on the Medical Research Council (MRC) UKALLXII/Eastern Cooperative Oncology Group (ECOG) 2993 trial.

A. Cherry, M. Tallman, S. Richards, 2005, Blood.

The t(6;11)(q27;q23) translocation in acute leukemia: a laboratory and clinical study of 30 cases

R. Berger, A. Moorman, A. Moorman, 1998, Leukemia.

The t(10;11)(p12;q23) translocation in acute leukaemia: a cytogenetic and clinical study of 20 patients

R. Berger, A. Moorman, B. Young, 1998, Leukemia.

Short communication Is trisomy 5 a distinct cytogenetic subgroup in acute lymphoblastic leukemia

C. Harrison, A. Moorman, M. Martineau, 2004 .

Graft-versus-leukemia effect in acute lymphoblastic leukemia: the importance of tumor burden and early detection

M. Loken, A. Moorman, C. Harrison, 2004, Leukemia.