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                             14 gevonden resultaten
nr titel auteur tijdschrift jaar jaarg. afl. pagina('s) type
1 A homozygote splice site PMS2 mutation as cause of Turcot syndrome gives rise to two different abnormal transcripts Sjursen, Wenche
2008
8 3 p. 179-186
artikel
2 Breast cancer immunohistochemistry can be useful in triage of some HNPCC families Shanley, S.
2009
8 3 p. 251-255
artikel
3 Consistency of self-reported first-degree family history of cancer in a population-based study Roth, Fernanda Lenara
2009
8 3 p. 195-202
artikel
4 Evidence of tumor microsatellite instability in gastric cancer with familial aggregation Pedrazzani, Corrado
2009
8 3 p. 215-220
artikel
5 Factors associated with intrusive cancer-related worries in women undergoing cancer genetic risk assessment Bennett, Paul
2009
8 3 p. 263
artikel
6 Familial nasopharyngeal carcinoma in Hong Kong: epidemiology and implication in screening Ng, Wai Tong
2009
8 3 p. 261-262
artikel
7 Haplotype and quantitative transcript analyses of Portuguese breast/ovarian cancer families with the BRCA1 R71G founder mutation of Galician origin Santos, Catarina
2008
8 3 p. 203-208
artikel
8 Health behaviors among Ashkenazi Jewish individuals receiving counseling for BRCA1 and BRCA2 mutations Quach, Jackie
2009
8 3 p. 241-250
artikel
9 Homozygosity of MSH2 c.1906G→C germline mutation is associated with childhood colon cancer, astrocytoma and signs of Neurofibromatosis type I Toledano, Helen
2008
8 3 p. 187-194
artikel
10 Lymphocyte recruitment into the tumor site is altered in patients with MSI-H colon cancer Drescher, Kristen M.
2009
8 3 p. 231-239
artikel
11 Men in the women’s world of hereditary breast and ovarian cancer—a systematic review Strømsvik, Nina
2009
8 3 p. 221-229
artikel
12 Response to neo-adjuvant chemotherapy in BRCA1 and BRCA2 related stage III breast cancer Hubert, Ayala
2008
8 3 p. 173-177
artikel
13 Sarcomas associated with hereditary nonpolyposis colorectal cancer: broad anatomical and morphological spectrum Nilbert, Mef
2009
8 3 p. 209-213
artikel
14 SDHB-associated renal oncocytoma suggests a broadening of the renal phenotype in hereditary paragangliomatosis Henderson, Alex
2009
8 3 p. 257-260
artikel
                             14 gevonden resultaten
 
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