Volume 5, Issue 2 | Familial Cancer

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Volume 5, Issue 2

June 2006

Breast Cancer Treatment and Genetics

Issue Editor:

Diana Eccles

15 articles in this issue

Part I Special Issue: Breast Cancer Treatment and Genetics

EditorialNotes Pages: I - I
Familial Cancer (special issue) Breast Cancer Treatment and Genetics
Diana M. Eccles
Editorial Pages: 127 - 128
Genotype Phenotype Correlation in Li-Fraumeni Syndrome Kindreds and its Implications for Management
R. N. Moule
S. G. Jhavar
R. A. Eeles
OriginalPaper Pages: 129 - 133
BRCA1 and BRCA2: Chemosensitivity, Treatment Outcomes and Prognosis
William D. Foulkes
OriginalPaper Pages: 135 - 142
Interleukin-10 Polymorphisms, Cancer Susceptibility and Prognosis
W. Martin Howell
Matthew J. Rose-Zerilli
OriginalPaper Pages: 143 - 149
Pharmacogenetics in the Management of Breast Cancer – Prospects for Individualised Treatment
Fiona H. Blackhall
Sacha Howell
Bill Newman
OriginalPaper Pages: 151 - 157
Part II Regular Articles

EditorialNotes Pages: 158 - 158
Determinants of Preferences for Genetic Counselling in Jewish Women
Carmel Apicella
Stuart J. Peacock
John L. Hopper
OriginalPaper Pages: 159 - 167
Late-Onset Common Cancers in a Kindred with an Arg213Gln TP53 Germline Mutation
Mariëlle W. G. Ruijs
Senno Verhoef
Fred H. Menko
OriginalPaper Pages: 169 - 174
Compliance and Satisfaction with Long-Term Surveillance in Finnish HNPCC Families
Kirsi Pylvänäinen
Matti Kairaluoma
Jukka-Pekka Mecklin
OriginalPaper Pages: 175 - 178
Germline Mutations of the hMLH1 and hMSH2 Mismatch Repair Genes in Belgian Hereditary Nonpolyposis Colon Cancer (HNPCC) Patients
M. Spaepen
B. Vankeirsbilck
G. Matthijs
OriginalPaper Pages: 179 - 189
Desmoid Tumors – a Characterization of Patients Seen at Mayo Clinic 1976–1999
Taya Fallen
Marcia Wilson
Noralane M Lindor
OriginalPaper Pages: 191 - 194
A ‘Nonsense’ Mutation Leads to Aberrant Splicing of hMLH1 in a German Hereditary Non-polyposis Colorectal Cancer Family
J. Baehring
C. Sutter
J. Gebert
OriginalPaper Pages: 195 - 199
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
Patrick J. Morrison
OriginalPaper Pages: 201 - 204
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
Andrew Silver
OriginalPaper Pages: 205 - 208