| nr |
titel |
auteur |
tijdschrift |
jaar |
jaarg. |
afl. |
pagina('s) |
type |
| 1 |
A polymorphism at miRNA-122-binding site in the IL-1α 3′UTR is associated with risk of epithelial ovarian cancer
|
Zhang, Zhu
|
|
2014
|
13 |
4 |
p. 595-601
|
artikel
|
| 2 |
A primary care audit of familial risk in patients with a personal history of breast cancer
|
Nathan, Paul
|
|
2014
|
13 |
4 |
p. 591-594
|
artikel
|
| 3 |
Association of interleukin-23 receptor gene polymorphisms with risk of bladder cancer in Chinese
|
Tang, Tielong
|
|
2014
|
13 |
4 |
p. 619-623
|
artikel
|
| 4 |
Association of reduced XRCC2 expression with lymph node metastasis in breast cancer tissues
|
Bashir, Nabiha
|
|
2014
|
13 |
4 |
p. 611-617
|
artikel
|
| 5 |
Cancer genetic testing panels for inherited cancer susceptibility: the clinical experience of a large adult genetics practice
|
Selkirk, Christina G.
|
|
2014
|
13 |
4 |
p. 527-536
|
artikel
|
| 6 |
Cribriform-morular variant of papillary thyroid carcinoma: an indication to screen for occult FAP
|
Levy, Rachel A.
|
|
2014
|
13 |
4 |
p. 547-551
|
artikel
|
| 7 |
Distinct gene expression profiles in ovarian cancer linked to Lynch syndrome
|
Jönsson, Jenny-Maria
|
|
2014
|
13 |
4 |
p. 537-545
|
artikel
|
| 8 |
Genetic 135G/C polymorphism of RAD51 gene and risk of cancer: a meta-analysis of 28,956 cases and 28,372 controls
|
Zhang, Bei-bei
|
|
2014
|
13 |
4 |
p. 515-526
|
artikel
|
| 9 |
Germline CDKN2A mutations in Brazilian patients of hereditary cutaneous melanoma
|
Ávila, Alexandre Leon Ribeiro de
|
|
2014
|
13 |
4 |
p. 645-649
|
artikel
|
| 10 |
Hereditary leiomyomatosis and renal cell cancer (HLRCC): renal cancer risk, surveillance and treatment
|
Menko, Fred H.
|
|
2014
|
13 |
4 |
p. 637-644
|
artikel
|
| 11 |
High prevalence of mismatch repair deficiency in prostate cancers diagnosed in mismatch repair gene mutation carriers from the colon cancer family registry
|
Rosty, Christophe
|
|
2014
|
13 |
4 |
p. 573-582
|
artikel
|
| 12 |
High-resolution melting (HRM) assay for the detection of recurrent BRCA1/BRCA2 germline mutations in Tunisian breast/ovarian cancer families
|
Riahi, Aouatef
|
|
2014
|
13 |
4 |
p. 603-609
|
artikel
|
| 13 |
“It’s all very well reading the letters in the genome, but it’s a long way to being able to write”: Men’s interpretations of undergoing genetic profiling to determine future risk of prostate cancer
|
Bancroft, Elizabeth K.
|
|
2014
|
13 |
4 |
p. 625-635
|
artikel
|
| 14 |
Molecular heterogeneity of familial myeloproliferative neoplasms revealed by analysis of the commonly acquired JAK2, CALR and MPL mutations
|
Langabeer, Stephen E.
|
|
2014
|
13 |
4 |
p. 659-663
|
artikel
|
| 15 |
Muir–Torre syndrome or phenocopy? The value of the immunohistochemical expression of mismatch repair proteins in sebaceous tumors of immunocompromised patients
|
Ponti, G.
|
|
2014
|
13 |
4 |
p. 553-561
|
artikel
|
| 16 |
Phenotype of SDHB mutation carriers in the Netherlands
|
Hulsteijn, Leonie T. van
|
|
2014
|
13 |
4 |
p. 651-657
|
artikel
|
| 17 |
Rapid and cost effective screening of breast and ovarian cancer genes using novel sequence capture method in clinical samples
|
Árvai, Kristóf
|
|
2014
|
13 |
4 |
p. 583-589
|
artikel
|
| 18 |
The secondary bile acid, deoxycholate accelerates intestinal adenoma–adenocarcinoma sequence in Apcmin/+ mice through enhancing Wnt signaling
|
Cao, Hailong
|
|
2014
|
13 |
4 |
p. 563-571
|
artikel
|
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