K. Cheung

发表

Retinoblastoma in association with the chromosome breakage syndromes Fanconi's anaemia and Bloom's syndrome: clinical and cytogenetic findings

J. Birch, C. Harrison, J. Hungerford, 1995, Clinical genetics.

Cytogenetics of multiple myeloma: interpretation of fluorescence in situ hybridization results

G. Gerrard, A. Mehta, K. L. Cheung, 2003, British journal of haematology.

Three distinct subgroups of hypodiploidy in acute lymphoblastic leukaemia

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

Outcome heterogeneity in childhood high-hyperdiploid acute lymphoblastic leukemia.

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

Deletion of chromosome 13 detected by conventional cytogenetics is a critical prognostic factor in myeloma

G. Morgan, N. Cross, F. Ross, 2006, Leukemia.

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.

Cytogenetic and genomic characterization of cell line ARH77.

C. Harrison, J. Strefford, H. Parker, 2008, Cancer genetics and cytogenetics.

Translocations of 14q32 and deletions of 13q14 are common chromosomal abnormalities in systemic amyloidosis

G. Gerrard, P. Hawkins, A. Mehta, 2002, British journal of haematology.

Frequent upregulation of MYC in plasma cell leukemia

N. Cross, H. White, C. Harrison, 2009, Genes, chromosomes & cancer.

t(14;19)(q32;q13): A recurrent translocation in B‐cell precursor acute lymphoblastic leukemia

C. Harrison, A. Moorman, H. Robinson, 2004, Genes, chromosomes & cancer.

Racial variation in incidence of trisomy 21: survey of 57,742 Chinese deliveries.

T. Lau, M. Rogers, K. Cheung, 1998, American journal of medical genetics.

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

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

Fluorescence in situ hybridisation studies to characterise complete and partial monosomy 7 in myeloid disorders

T. Lister, L. Kearney, B. Young, 1994, Genes, chromosomes & cancer.

Investigation of the clonality and minimal residual disease in haematological malignancy using fluorescence in situ hybridization.

A. Kasprzyk, L. Foroni, C. Bishop, 1998 .

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

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

Preoperative endocrine therapy for breast cancer.

A. Howell, K. Cheung, J. Robertson, 2000, Endocrine-related cancer.