F. Ross

发表

Identification of false-positive CBFβ/MYH11 RT-PCR results

S. Hackwell, DO Robinson, J. Harvey, 1999, Leukemia.

Characterization of a highly complex region in Xq13 and mapping of three isodicentric breakpoints associated with preleukemia.

A. Monaco, J. Ramser, R. Reinhardt, 2000, Genomics.

Trisomy 15 associated with loss of the Y chromosome in bone marrow: a possible new aging effect.

E. J. Sinclair, A. Watmore, E J Sinclair, 1998, Cancer genetics and cytogenetics.

A novel 3′ mutation in the APC gene in a family presenting with a desmoid tumour

A. Bateman, D. Eccles, F. Ross, 2001, Journal of medical genetics.

Characterization of a new non-Hodgkin's lymphoma cell line (NCEB-1) with a chromosomal (11:14) translocation [t(11:14)(q13;q32)].

C. M. Steel, C. Ludlam, D. Saltman, 1988, Blood.

Comparative genomic hybridization and histological variation in primitive neuroectodermal tumours

D. Ellison, J. Nicholson, J. Kohler, 1999, British Journal of Cancer.

A new in vivo and in vitro B cell lymphoma model, pi-BCL1.

T. Illidge, W. Howatt, J. Honeychurch, 2000, Cancer biotherapy & radiopharmaceuticals.

Disruption and aberrant expression of HMGA2 as a consequence of diverse chromosomal translocations in myeloid malignancies

M. Odero, M. Calasanz, J. Vizmanos, 2005, Leukemia.

Comparative genomic hybridization (CGH) analysis of stage 4 neuroblastoma reveals high frequency of 11q deletion in tumors lacking MYCN amplification

F. Speleman, J. Vandesompele, O. Delattre, 2001, International journal of cancer.

Imbalances of chromosome 17 in medulloblastomas determined by comparative genomic hybridisation and fluorescence in situ hybridisation

J. Crolla, D. Ellison, J. Nicholson, 2000, Molecular pathology : MP.

Karyotypic abnormalities and immunoglobulin gene rearrangements in Hodgkin's disease.

S. Gledhill, R. Banks, A. Krajewski, 1991, Cancer genetics and cytogenetics.

Hematological features of patients with myelodysplastic syndromes associated with a chromosome 5q deletion

J Boultwood, D. Oscier, F. Ross, 1995, American journal of hematology.

Multicentre analysis of patterns of DNA gains and losses in 204 neuroblastoma tumors: how many genetic subgroups are there?

F. Speleman, J. Vandesompele, O. Delattre, 2001, Medical and pediatric oncology.

Genetic abnormalities detected in ependymomas by comparative genomic hybridisation

R. Allibone, J. Crolla, D. Ellison, 2002, British Journal of Cancer.

Patients with essential thrombocythemia do not express BCR-ABL transcripts.

S. Hackwell, F. Ross, J. Cullis, 1999, Blood.

Cytogenetically cryptic AML1–ETO and CBFβ–MYH11 gene rearrangements: incidence in 412 cases of acute myeloid leukaemia

J. Reilly, G. Wilson, A. Watmore, 2000, British journal of haematology.

A novel 3' mutation in the APC gene in a family presenting with a desmoid tumour.

A. Bateman, D. Eccles, F. Ross, 2001, Journal of medical genetics.