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Intra-individual variation in G2 chromosomal radiosensitivity

Mutagenesis, 2012-07, Vol.27 (4), p.471-475

2012

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G2 checkpoint control and G2 chromosomal radiosensitivity in cancer survivors and their families

Mutagenesis, 2011-03, Vol.26 (2), p.291-294

2011

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Comparison of germ line minisatellite mutation detection at the CEB1 locus by Southern blotting and PCR amplification

Mutagenesis, 2010-07, Vol.25 (4), p.343-349

2010

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Chromosomal Abnormalities among Offspring of Childhood-Cancer Survivors in Denmark: A Population-Based Study

American journal of human genetics, 2004-06, Vol.74 (6), p.1282-1285

2004

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Mitochondrial DNA mutation frequencies in experimentally irradiated compost worms, Eisenia fetida

Mutation research, 2006-01, Vol.603 (1), p.56-63

2006

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Genetic effects of radiotherapy for childhood cancer

Health physics (1958), 2003-07, Vol.85 (1), p.65

2003

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Chromosome analysis in childhood cancer survivors and their offspring—No evidence for radiotherapy-induced persistent genomic instability

Mutation research, 2005-06, Vol.583 (2), p.198-206

2005

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Influence of polymorphisms at loci encoding DNA repair proteins on cancer susceptibility and G2 chromosomal radiosensitivity

Environmental and molecular mutagenesis, 2007-01, Vol.48 (1), p.48-57

2007

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Biological dosimetry of radiation workers at the Sellafield nuclear facility

Radiation research, 1997-09, Vol.148 (3), p.216

1997

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Thymidylate synthase repeat polymorphisms and risk of neural tube defects in a population from the northern United Kingdom

Birth defects research. A Clinical and molecular teratology, 2004-07, Vol.70 (7), p.483-485

2004

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Somatic Cell Mutations at the Glycophorin A Locus in Erythrocytes of Radiation Workers from the Sellafield Nuclear Facility

Radiation research, 2003-01, Vol.159 (1), p.117-122

2003

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study of DNA damage recognition and repair gene polymorphisms in relation to cancer predisposition and G₂ chromosomal radiosensitivity

Environmental and molecular mutagenesis, 2011, Vol.52 (1), p.72-76

2011

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A de novo interstitial deletion of 15(q21.2q22.1) in a moderately retarded adult male

Journal of medical genetics, 1990-10, Vol.27 (10), p.637-639

1990

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Frequencies of chromosome aberrations in a control population determined by G banding

Mutation research, 2001-02, Vol.490 (2), p.171-177

2001

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Sequential chromosome aberration analysis following radiotherapy — no evidence for enhanced genomic instability

Mutation research, 2000-02, Vol.465 (1), p.45-51

2000

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The North Cumbria Community Genetics Project

Journal of medical genetics, 1998-05, Vol.35 (5), p.413-416

1998

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Chromosome Studies in Plutonium Workers

International journal of radiation biology, 1985-01, Vol.47 (5), p.599-610

1985

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Chromosome aberrations in radiation workers with internal deposits of plutonium

Radiation research, 1998-10, Vol.150 (4), p.459

1998

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Individual variation in somatic mutations of the glycophorin-A gene in neonates in relation to pre-natal factors

Mutation research, 2000-05, Vol.467 (2), p.153-159

2000

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The non-random occurrence of exchanges involving chromosomes 7 and 14 in human lymphocytes: a prospective study of control individuals

Mutation research, 1988-05, Vol.199 (1), p.215-220

Tawn, E J

1988

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A cytogenetic study of men occupationally exposed to uranium

British Journal of Industrial Medicine, 1991-02, Vol.48 (2), p.98-102

1991

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The effect of smoking on the frequencies of asymmetrical and symmetrical chromosome exchanges in human lymphocytes

Mutation Research/Genetic Toxicology, 1989-10, Vol.224 (2), p.151-156

1989

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The frequencies of constitutional chromosome abnormalities in an apparently normal adult population

Mutation research, 1992-09, Vol.283 (1), p.69-73

1992

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Cells with multiple chromosome aberrations in control individuals

Mutation research, 1985-12, Vol.144 (4), p.247-250

1985

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Intra-individual variation in G2 chromosomal radiosensitivity

G2 checkpoint control and G2 chromosomal radiosensitivity in cancer survivors and their families

Comparison of germ line minisatellite mutation detection at the CEB1 locus by Southern blotting and PCR amplification

Chromosomal Abnormalities among Offspring of Childhood-Cancer Survivors in Denmark: A Population-Based Study

Mitochondrial DNA mutation frequencies in experimentally irradiated compost worms, Eisenia fetida

Genetic effects of radiotherapy for childhood cancer

Chromosome analysis in childhood cancer survivors and their offspring—No evidence for radiotherapy-induced persistent genomic instability

Influence of polymorphisms at loci encoding DNA repair proteins on cancer susceptibility and G2 chromosomal radiosensitivity

Biological dosimetry of radiation workers at the Sellafield nuclear facility

Thymidylate synthase repeat polymorphisms and risk of neural tube defects in a population from the northern United Kingdom

Somatic Cell Mutations at the Glycophorin A Locus in Erythrocytes of Radiation Workers from the Sellafield Nuclear Facility

study of DNA damage recognition and repair gene polymorphisms in relation to cancer predisposition and G₂ chromosomal radiosensitivity

A de novo interstitial deletion of 15(q21.2q22.1) in a moderately retarded adult male

Frequencies of chromosome aberrations in a control population determined by G banding

Sequential chromosome aberration analysis following radiotherapy — no evidence for enhanced genomic instability

The North Cumbria Community Genetics Project

Chromosome Studies in Plutonium Workers

Chromosome aberrations in radiation workers with internal deposits of plutonium

Individual variation in somatic mutations of the glycophorin-A gene in neonates in relation to pre-natal factors

The non-random occurrence of exchanges involving chromosomes 7 and 14 in human lymphocytes: a prospective study of control individuals

A cytogenetic study of men occupationally exposed to uranium

The effect of smoking on the frequencies of asymmetrical and symmetrical chromosome exchanges in human lymphocytes

The frequencies of constitutional chromosome abnormalities in an apparently normal adult population

Cells with multiple chromosome aberrations in control individuals

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