M. Fitchett

发表

Prognostic factors in stage AO B‐cell chronic lymphocytic leukaemia

D. Oscier, R. Pickering, T. Hamblin, 1990, British journal of haematology.

Characterization of three de novo derivative chromosomes 16 by "reverse chromosome painting" and molecular analysis.

J. Armour, P. Harris, P. Rudd, 1993, American journal of human genetics.

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.

Karyotypic evolution in B‐cell chronic lymphocytic leukaemia

D. Oscier, M. Fitchett, T. Herbert, 1991, Genes, chromosomes & cancer.

Neurofibromatosis and childhood leukaemia/lymphoma: a population-based UKCCSG study.

C. Stiller, J. Chessells, M. Fitchett, 1994, British Journal of Cancer.

Hirschsprung's disease associated with a deletion of chromosome 10 (q11.2q21.2): a further link with the neurocristopathies?

S. Huson, L. Mulligan, P. Tam, 1994, Journal of medical genetics.

The association of Angelman's syndrome with deletions within 15q11-13.

M. Pembrey, C. Clarke, M. Super, 1989, Journal of medical genetics.

An economic appraisal of alternative pre-natal screening programmes for Down's syndrome.

P. Shackley, A. Mcguire, M. Roche, 1993, Journal of public health medicine.

Characterization ofThreeDeNovoDerivative Chromosomes 16by"Reverse ChromosomePainting" andMolecular Analysis

J. Armour, P. Harris, P. Rudd, 1993 .

Comparison of cytogenetic and restriction fragment length polymorphism analyses for the detection of loss of chromosome material in clonal hemopoietic disorders

D. Oscier, V. Buckle, J. Wainscoat, 1993, American journal of hematology.

Complete and partial XY sex reversal associated with terminal deletion of 10q: report of 2 cases and literature review.

S. Huson, A. Wilkie, R. Daniels, 1993, American journal of medical genetics.

Molecular Cytogenetic Analysis of 7q Abnormalities in Acute Leukemia

L. Kearney, J. Harbott, A. Biondi, 1997 .

Prognostic subgroups in B-cell chronic lymphocytic leukemia defined by specific chromosomal abnormalities.

S. Knuutila, G. Gahrton, G. Juliusson, 1990, The New England journal of medicine.

Acute meningo-encephalitis due to amoebae of the order myxomycetale (slime mould).

M. Fitchett, D. Pullon, J. Malloch, 1970, The New Zealand medical journal.

Chromosome Abnormalities and Genetic Counselling

D. Love, E. Whittle, S. Bundey, 1990 .

Cytogenetic Findings and Survival in B-cell Chronic Lymphocytic Leukemia. Second IWCCLL Compilation of Data on 662 Patients.

P. Nowell, S. Knuutila, G. Gahrton, 1991, Leukemia & lymphoma.

Solid tissue culture for cytogenetic analysis: a collaborative survey for the Association of Clinical Cytogeneticists.

M. Creasy, M. Fitchett, J. Waters, 1996, Journal of clinical pathology.

The behaviour of fragile X and other aberrations during recovery from low folate conditions

J. Savage, M. Fitchett, 2004, Chromosoma.

Del(18p) shown to be a cryptic translocation using a multiprobe FISH assay for subtelomeric chromosome rearrangements.

J. Flint, S. Knight, L. Kearney, 1998, Journal of medical genetics.

population-based UKCCSG study

C. Stiller, J. Chessells, M. Fitchett, 1994 .

Constitutional and acquired trisomy 8.

L. Secker-Walker, M. Fitchett, L. Secker‐Walker, 1995, Leukemia research.

Chromosome abnormalities involving band 13q14 in hematologic malignancies.

M. Seabright, D. Oscier, M. Fitchett, 1987, Cancer genetics and cytogenetics.

Correlation of chromosome abnormalities with laboratory features and clinical course in B‐cell chronic lymphocytic leukaemia

D. Oscier, R. Pickering, T. Hamblin, 1990, British journal of haematology.

Chromosomal abnormalities in B-CLL.

D. Oscier, T. Hamblin, M. Fitchett, 1988, Nouvelle revue francaise d'hematologie.

Detection of chromosomal 7 loss in myelodysplasia using an extremely polymorphic DNA probe.

A. Jeffreys, D. Oscier, S. Thein, 1988, British Journal of Cancer.

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

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

Interstitial deletion of distal 13q associated with Hirschsprung's disease.

N. Dennis, M. Fitchett, M. Lamont, 1989, Journal of medical genetics.

Molecular studies of the fragile X syndrome.

S. Knight, S. Huson, A. Roche, 1992, American journal of medical genetics.

Deleted X chromosomes in patients with the fragile X syndrome.

M. Seabright, M. Fitchett, 1984, Journal of medical genetics.

Polycythaemia rubra vera and hairy cell leukaemia in the same patient: studies on the spleen

F. Stevenson, G. Mufti, T. Hamblin, 1982, Journal of clinical pathology.

A new parental cell line for human x human hybridoma production

M. Fitchett, S. Clark, S. James, 1988, Cytotechnology.

Two 46,XX,t(X;Y) females with linear skin defects and congenital microphthalmia: a new syndrome at Xp22.3.

L. Al-Gazali, R. Mueller, A. McCartney, 1990, Journal of medical genetics.

Interstitial deletion of band 3q25.

S. Huson, A. Slavotinek, M. Fitchett, 1997, Journal of medical genetics.

Two46,XX,t(X;Y) females withlinear skin defects and congenital microphthalmia: a new syndrome atXp22.3

R. Mueller, A. McCartney, A. Caine, 1990 .

Prenatal diagnosis of cri du chat (5p‐) syndrome in association with isolated moderate bilateral ventriculomegaly

M. Crocker, M. Fitchett, E. Stefanou, 2002, Prenatal diagnosis.

FRA(X)(p22) NOT ASSOCIATED WITH INFANTILE AUTISM

W. Brown, S. Nolin, M. Fitchett, 1984, The Lancet.