Issue 2/2006
Breast Cancer Treatment and Genetics
Content (15 Articles)
Genotype Phenotype Correlation in Li-Fraumeni Syndrome Kindreds and its Implications for Management
R. N. Moule, S. G. Jhavar, R. A. Eeles
Interleukin-10 Polymorphisms, Cancer Susceptibility and Prognosis
W. Martin Howell, Matthew J. Rose-Zerilli
Pharmacogenetics in the Management of Breast Cancer – Prospects for Individualised Treatment
Fiona H. Blackhall, Sacha Howell, Bill Newman
Determinants of Preferences for Genetic Counselling in Jewish Women
Carmel Apicella, Stuart J. Peacock, Lesley Andrews, Katherine Tucker, Agnes Bankier, Mary B. Daly, John L. Hopper
Late-Onset Common Cancers in a Kindred with an Arg213Gln TP53 Germline Mutation
Mariëlle W. G. Ruijs, Senno Verhoef, Gea Wigbout, Roelof Pruntel, Arno N. Floore, Daphne de Jong, Laura J. van ′t Veer, Fred H. Menko
Compliance and Satisfaction with Long-Term Surveillance in Finnish HNPCC Families
Kirsi Pylvänäinen, Matti Kairaluoma, Jukka-Pekka Mecklin
Germline Mutations of the hMLH1 and hMSH2 Mismatch Repair Genes in Belgian Hereditary Nonpolyposis Colon Cancer (HNPCC) Patients
M. Spaepen, B. Vankeirsbilck, S. Van Opstal, S. Tejpar, E. Van Cutsem, K. Geboes, E. Legius, G. Matthijs
Desmoid Tumors – a Characterization of Patients Seen at Mayo Clinic 1976–1999
Taya Fallen, Marcia Wilson, Bruce Morlan, Noralane M Lindor
A ‘Nonsense’ Mutation Leads to Aberrant Splicing of hMLH1 in a German Hereditary Non-polyposis Colorectal Cancer Family
J. Baehring, C. Sutter, M. Kadmon, M. V. Knebel Doeberitz, J. Gebert
The RET Mutation E768D Confers a Late-onset Familial Medullary Thyroid Carcinoma – Only Phenotype with Incomplete Penetrance: Implications for Screening and Management of Carrier Status
Tabib Dabir, Steven J. Hunter, Colin F. J. Russell, Damien McCall, Patrick J. Morrison
A Novel Exon Duplication Event Leading to a Truncating Germ-line Mutation of the APC Gene in a Familial Adenomatous Polyposis Family
Amy McCart, Andrew Latchford, Emmanouil Volikos, Andrew Rowan, Ian Tomlinson, Andrew Silver