| nr |
titel |
auteur |
tijdschrift |
jaar |
jaarg. |
afl. |
pagina('s) |
type |
| 1 |
A ‘Nonsense’ Mutation Leads to Aberrant Splicing of hMLH1 in a German Hereditary Non-polyposis Colorectal Cancer Family
|
Baehring, J.
|
|
2006
|
5 |
2 |
p. 195-199
|
artikel
|
| 2 |
A Novel Exon Duplication Event Leading to a Truncating Germ-line Mutation of the APC Gene in a Familial Adenomatous Polyposis Family
|
McCart, Amy
|
|
2006
|
5 |
2 |
p. 205-208
|
artikel
|
| 3 |
BRCA1 and BRCA2: Chemosensitivity, Treatment Outcomes and Prognosis
|
Foulkes, William D.
|
|
2006
|
5 |
2 |
p. 135-142
|
artikel
|
| 4 |
Compliance and Satisfaction with Long-Term Surveillance in Finnish HNPCC Families
|
Pylvänäinen, Kirsi
|
|
2006
|
5 |
2 |
p. 175-178
|
artikel
|
| 5 |
Desmoid Tumors – a Characterization of Patients Seen at Mayo Clinic 1976–1999
|
Fallen, Taya
|
|
2006
|
5 |
2 |
p. 191-194
|
artikel
|
| 6 |
Determinants of Preferences for Genetic Counselling in Jewish Women
|
Apicella, Carmel
|
|
2006
|
5 |
2 |
p. 159-167
|
artikel
|
| 7 |
Familial Cancer (special issue) Breast Cancer Treatment and Genetics
|
Eccles, Diana M.
|
|
2006
|
5 |
2 |
p. 127-128
|
artikel
|
| 8 |
Genotype Phenotype Correlation in Li-Fraumeni Syndrome Kindreds and its Implications for Management
|
Moule, R. N.
|
|
2006
|
5 |
2 |
p. 129-133
|
artikel
|
| 9 |
Germline Mutations of the hMLH1 and hMSH2 Mismatch Repair Genes in Belgian Hereditary Nonpolyposis Colon Cancer (HNPCC) Patients
|
Spaepen, M.
|
|
2006
|
5 |
2 |
p. 179-189
|
artikel
|
| 10 |
Interleukin-10 Polymorphisms, Cancer Susceptibility and Prognosis
|
Howell, W. Martin
|
|
2006
|
5 |
2 |
p. 143-149
|
artikel
|
| 11 |
Late-Onset Common Cancers in a Kindred with an Arg213Gln TP53 Germline Mutation
|
Ruijs, Mariëlle W. G.
|
|
2006
|
5 |
2 |
p. 169-174
|
artikel
|
| 12 |
Part II Regular Articles
|
|
|
2006
|
5 |
2 |
p. 158
|
artikel
|
| 13 |
Part I Special Issue: Breast Cancer Treatment and Genetics
|
|
|
2006
|
5 |
2 |
p. I
|
artikel
|
| 14 |
Pharmacogenetics in the Management of Breast Cancer – Prospects for Individualised Treatment
|
Blackhall, Fiona H.
|
|
2006
|
5 |
2 |
p. 151-157
|
artikel
|
| 15 |
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
|
Dabir, Tabib
|
|
2006
|
5 |
2 |
p. 201-204
|
artikel
|
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