| nr |
titel |
auteur |
tijdschrift |
jaar |
jaarg. |
afl. |
pagina('s) |
type |
| 1 |
BRCA1 testing
|
Górski, Bohdan
|
|
2008
|
|
2 |
p. 81-82
|
artikel
|
| 2 |
Case Report: Familial Gastric Cancer and Chordoma in the Same Family
|
Weber, Walter
|
|
2005
|
|
2 |
p. 81-84
|
artikel
|
| 3 |
Childhood Adrenocortical Tumours: a Review
|
Marques-Pereira, Rosana
|
|
2006
|
|
2 |
p. 81-89
|
artikel
|
| 4 |
Clinical, Molecular and Geographical Features of Hereditary Breast/Ovarian Cancer in Latvia
|
Gardovskis, Andris
|
|
2005
|
|
2 |
p. 71-76
|
artikel
|
| 5 |
Clinical Outcome of Hereditary Breast Cancer in the Lithuanian Population
|
Elsakov, Pavel
|
|
2005
|
|
2 |
p. 77-79
|
artikel
|
| 6 |
Colorectal Cancer in the Family: Psychosocial Distress and Social Issues in the Years Following Genetic Counselling
|
Bleiker, Eveline MA
|
|
2007
|
|
2 |
p. 59-66
|
artikel
|
| 7 |
Colorectal Tumour Microsatellite Instability Test Results: Perspectives from Patients
|
Lindor, Noralane M
|
|
2004
|
|
2 |
p. 69-75
|
artikel
|
| 8 |
Comment on the article Genetic contribution to all cancers: the first demonstration using the model of breast cancers from Poland stratified by age at diagnosis and tumour pathology by Lubinski et al., Breast Cancer Res Treat 2008 Apr 15
|
Irmejs, Arvids
|
|
2008
|
|
2 |
p. 66-66
|
artikel
|
| 9 |
Developments in Clinical Practice: Follow up Clinic for BRCA Mutation Carriers: a Case Study Highlighting the "Virtual Clinic"
|
Ardern-Jones, Audrey
|
|
2004
|
|
2 |
p. 77-79
|
artikel
|
| 10 |
DNA and RNA analyses in detection of genetic predisposition to cancer
|
Matyjasik, Joanna
|
|
2008
|
|
2 |
p. 73-80
|
artikel
|
| 11 |
DNA testing for variants conferring low or moderate increase in the risk of cancer
|
Kurzawski, Grzegorz
|
|
2008
|
|
2 |
p. 84-87
|
artikel
|
| 12 |
Effect of Prior Bilateral Oophorectomy on the Presentation of Breast Cancer in BRCA1 and BRCA2 Mutation Carriers
|
Metcalfe, Kelly A
|
|
2005
|
|
2 |
p. 53-57
|
artikel
|
| 13 |
Epimutations, Inheritance and Causes of Aberrant DNA Methylation in Cancer
|
Mossman, David
|
|
2006
|
|
2 |
p. 75-80
|
artikel
|
| 14 |
Familial Cervical Cancer: Case Reports, Review and Clinical Implications
|
Zoodsma, Margreet
|
|
2004
|
|
2 |
p. 99-105
|
artikel
|
| 15 |
Familial Multiple Myeloma: Report on Two Families and Discussion of Screening Options
|
Gerkes, Erica H
|
|
2007
|
|
2 |
p. 72-78
|
artikel
|
| 16 |
Frequency of the Common MYH Mutations (G382D and Y165C) in MMR Mutation Positive and Negative HNPCC Patients
|
Ashton, Katie A
|
|
2005
|
|
2 |
p. 65-70
|
artikel
|
| 17 |
Gene Expression Profiling in Familial Adenomatous Polyposis Adenomas and Desmoid Disease
|
Bowden, Nikola A
|
|
2007
|
|
2 |
p. 79-96
|
artikel
|
| 18 |
Gene Expression Profiling of Xeroderma Pigmentosum
|
Bowden, Nikola A
|
|
2006
|
|
2 |
p. 103-110
|
artikel
|
| 19 |
Genetic Screening for Familial Gastric Cancer
|
Oliveira, Carla
|
|
2004
|
|
2 |
p. 51-64
|
artikel
|
| 20 |
Germline Missense Changes in the APC Gene and Their Relationship to Disease
|
Scott, Rodney J
|
|
2004
|
|
2 |
p. 81-91
|
artikel
|
| 21 |
Hereditary breast and ovarian cancer
|
Gronwald, Jacek
|
|
2008
|
|
2 |
p. 88-98
|
artikel
|
| 22 |
IMPACT and AIDIT: Strengthening Research Ties in Eastern Europe
|
Morgan, Sarah
|
|
2006
|
|
2 |
p. 111-112
|
artikel
|
| 23 |
Lynch syndrome (HNPCC)
|
Kładny, Józef
|
|
2008
|
|
2 |
p. 99-102
|
artikel
|
| 24 |
MSH2 and MLH1 testing
|
Kurzawski, Grzegorz
|
|
2008
|
|
2 |
p. 83-83
|
artikel
|
| 25 |
MSH6 syndrome
|
Suchy, Janina
|
|
2008
|
|
2 |
p. 103-104
|
artikel
|
| 26 |
Mutations in the von Hippel-Lindau Tumour Suppressor Gene in Central Nervous System Hemangioblastomas
|
Cybulski, Cezary
|
|
2004
|
|
2 |
p. 93-97
|
artikel
|
| 27 |
MUTYH Mutations Do Not Cause HNPCC or Late Onset Familial Colorectal Cancer
|
Stormorken, Astrid
|
|
2006
|
|
2 |
p. 90-93
|
artikel
|
| 28 |
No Sib Pair Concordance for Breast or Ovarian Cancer in BRCA1 Mutation Carriers
|
Møller, Pål
|
|
2007
|
|
2 |
p. 67-71
|
artikel
|
| 29 |
Nuclear Pedigree Criteria for the Identification of Individuals Suspected to Be at Risk of an Inherited Predisposition to Gastric Cancer
|
Gawdis-Wojnarska, Beata
|
|
2004
|
|
2 |
p. 65-68
|
artikel
|
| 30 |
Opinion on moderate/low cancer genetic risk markers in medical practice
|
Aretz, Stefan
|
|
2008
|
|
2 |
p. 61-63
|
artikel
|
| 31 |
Opinion on moderate/low cancer genetic risk markers in medical practice including comment on the article Genetic contribution to all cancers: the first demonstration using the model of breast cancers from Poland stratified by age at diagnosis and tumour pathology by Lubinski et al., Breast Cancer Res Treat 2008 Apr 15
|
Costa, Sandra
|
|
2008
|
|
2 |
p. 64-65
|
artikel
|
| 32 |
Other short opinions/comments on moderate/low cancer genetic risk markers in medical practice and the article Genetic contribution to all cancers: the first demonstration using the model of breast cancers from Poland stratified by age at diagnosis and tumour pathology by Lubinski et al., Breast Cancer Res Treat 2008 Apr 15
|
Aittomäki, Kristiina
|
|
2008
|
|
2 |
p. 67-68
|
artikel
|
| 33 |
Principles of genetic predisposition to malignancies
|
Dębniak, Tadeusz
|
|
2008
|
|
2 |
p. 69-72
|
artikel
|
| 34 |
Some Molecular and Clinical Aspects of Genetic Predisposition to Malignant Melanoma and Tumours of Various Site of Origin
|
Dębniak, Tadeusz
|
|
2007
|
|
2 |
p. 97-116
|
artikel
|
| 35 |
The Association of the COMT V158M Polymorphism with Endometrial/Ovarian Cancer in HNPCC Families Adhering to the Amsterdam Criteria
|
Ashton, Katie A
|
|
2006
|
|
2 |
p. 94-102
|
artikel
|
| 36 |
The 3020insC Allele of NOD2 Predisposes to Cancers of Multiple Organs
|
Lubiński, Jan
|
|
2005
|
|
2 |
p. 59-63
|
artikel
|
Tijdschrift beschrijving