J. M. Birch

发表

Relative frequency and morphology of cancers in carriers of germline TP53 mutations

J. Varley, J. Birch, A. Kelsey, 2001, Oncogene.

Is CHEK2 a cause of the Li–Fraumeni syndrome?

D. Evans, S. Narod, J. Birch, 2007, Journal of Medical Genetics.

Malignant transformation and new primary tumours after therapeutic radiation for benign disease: substantial risks in certain tumour prone syndromes

D. Evans, R. Ramsden, J. Birch, 2005, Journal of Medical Genetics.

Are there low-penetrance TP53 Alleles? evidence from childhood adrenocortical tumors.

D. Evans, J. Varley, G. Margison, 1999, American journal of human genetics.

Cancer phenotype correlates with constitutional TP53 genotype in families with the Li–Fraumeni syndrome

D. Evans, J. Varley, J. Birch, 1998, Oncogene.

Germ-line mutations of TP53 in Li-Fraumeni families: an extended study of 39 families.

D. Evans, J. Varley, M. Santibanez-Koref, 1997, Cancer research.

Are germ cell tumors part of the Li-Fraumeni cancer family syndrome?

H. B. Marsden, M. Teare, J. Birch, 1989, Cancer genetics and cytogenetics.

Heterozygous germ line hCHK2 mutations in Li-Fraumeni syndrome.

K. Isselbacher, J. Fraumeni, D. Haber, 1999, Science.

Childhood Acute Lymphoblastic Leukemia and Infections in the First Year of Life : A Report from the United Kingdom Childhood Cancer Study

P Ansell, E Roman, P A McKinney, 2007 .

Infectious exposure in the first year of life and risk of central nervous system tumors in children: analysis of day care, social contact, and overcrowding

J. Birch, P. McKinney, S. Hepworth, 2009, Cancer Causes & Control.

Retinoblastoma in Great Britain 1963–2002

G. Draper, C. Stiller, J. Birch, 2008, British Journal of Ophthalmology.

Prevalence and diversity of constitutional mutations in the p53 gene among 21 Li-Fraumeni families.

A. Craft, M. Santibanez-Koref, P. H. Jones, 1994, Cancer research.