| nr |
titel |
auteur |
tijdschrift |
jaar |
jaarg. |
afl. |
pagina('s) |
type |
| 1 |
An Ashkenazi founder mutation in the MSH6 gene leading to HNPCC
|
Goldberg, Yael
|
|
2009
|
9 |
2 |
p. 141-150
|
artikel
|
| 2 |
A PALB2 germline mutation associated with hereditary breast cancer in Italy
|
Papi, Laura
|
|
2009
|
9 |
2 |
p. 181-185
|
artikel
|
| 3 |
Biallelic MYH germline mutations as cause of Muir-Torre syndrome
|
Guillén-Ponce, Carmen
|
|
2009
|
9 |
2 |
p. 151-154
|
artikel
|
| 4 |
Clinical and histomolecular endometrial tumor characterization of patients at-risk for Lynch syndrome in South of Brazil
|
Cossio, Silvia Liliana
|
|
2009
|
9 |
2 |
p. 131-139
|
artikel
|
| 5 |
Efficiency of BRCAPRO and Myriad II mutation probability thresholds versus cancer history criteria alone for BRCA1/2 mutation detection
|
Harssel, J. J. T. van
|
|
2009
|
9 |
2 |
p. 193-201
|
artikel
|
| 6 |
Erratum to: FAP-associated desmoid invasiveness correlates with in vitro resistance to doxorubicin
|
Joyner, David E.
|
|
2009
|
9 |
2 |
p. 261
|
artikel
|
| 7 |
Evaluating Lynch syndrome in very early onset colorectal cancer probands without apparent polyposis
|
Jasperson, Kory W.
|
|
2009
|
9 |
2 |
p. 99-107
|
artikel
|
| 8 |
Evolving perspectives on genetic discrimination in health insurance among health care providers
|
Huizenga, Carin R.
|
|
2009
|
9 |
2 |
p. 253-260
|
artikel
|
| 9 |
Female BRCA mutation carriers with a preference for prophylactic mastectomy are more likely to participate an educational-support group and to proceed with the preferred intervention within 2 years
|
Landsbergen, Karin M.
|
|
2009
|
9 |
2 |
p. 213-220
|
artikel
|
| 10 |
Frequent alterations of the PI3K/AKT/mTOR pathways in hereditary nonpolyposis colorectal cancer
|
Ekstrand, Anna Isinger
|
|
2009
|
9 |
2 |
p. 125-129
|
artikel
|
| 11 |
Hereditary leiomyomatosis and renal cell carcinoma: very early diagnosis of renal cancer in a paediatric patient
|
Alrashdi, Ismail
|
|
2009
|
9 |
2 |
p. 239-243
|
artikel
|
| 12 |
Heredity, diet and lifestyle as determining risk factors for the esophageal cancer on Nanao Island in Southern China
|
Liu, Min
|
|
2009
|
9 |
2 |
p. 229-238
|
artikel
|
| 13 |
Heterogeneous prevalence of recurrent BRCA1 and BRCA2 mutations in Spain according to the geographical area: implications for genetic testing
|
Diez, Orland
|
|
2009
|
9 |
2 |
p. 187-191
|
artikel
|
| 14 |
Mismatch repair protein expression and colorectal cancer in Hispanics from Puerto Rico
|
De Jesus-Monge, Wilfredo E.
|
|
2009
|
9 |
2 |
p. 155-166
|
artikel
|
| 15 |
Mutation analysis of the APC gene in Taiwanese FAP families: low incidence of APC germline mutation in a distinct subgroup of FAP families
|
Chiang, J. M.
|
|
2009
|
9 |
2 |
p. 117-124
|
artikel
|
| 16 |
No evidence for a genetic modifier for renal cell cancer risk in HLRCC syndrome
|
Vahteristo, Pia
|
|
2009
|
9 |
2 |
p. 245-251
|
artikel
|
| 17 |
Outcomes of nasopharyngeal carcinoma screening for high risk family members in Hong Kong
|
Ng, Wai Tong
|
|
2009
|
9 |
2 |
p. 221-228
|
artikel
|
| 18 |
Recommendations to improve identification of hereditary and familial colorectal cancer in Europe
|
Vasen, H. F. A.
|
|
2009
|
9 |
2 |
p. 109-115
|
artikel
|
| 19 |
Retrospective comparison of patient outcomes after in-person and telephone results disclosure counseling for BRCA1/2 genetic testing
|
Doughty Rice, Courtney
|
|
2009
|
9 |
2 |
p. 203-212
|
artikel
|
| 20 |
Selection of patients with germline MLH1 mutated Lynch syndrome by determination of MLH1 methylation and BRAF mutation
|
Bouzourene, Hanifa
|
|
2009
|
9 |
2 |
p. 167-172
|
artikel
|
| 21 |
Serum antibodies against frameshift peptides in microsatellite unstable colorectal cancer patients with Lynch syndrome
|
Reuschenbach, Miriam
|
|
2009
|
9 |
2 |
p. 173-179
|
artikel
|
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