| nr |
titel |
auteur |
tijdschrift |
jaar |
jaarg. |
afl. |
pagina('s) |
type |
| 1 |
Cancer risk and genotype–phenotype correlations in PTEN hamartoma tumor syndrome
|
Nieuwenhuis, Marry H.
|
|
2013
|
13 |
1 |
p. 57-63
|
artikel
|
| 2 |
Cancer risk and overall survival in mismatch repair proficient hereditary non-polyposis colorectal cancer, Lynch syndrome and sporadic colorectal cancer
|
Garre, Pilar
|
|
2013
|
13 |
1 |
p. 109-119
|
artikel
|
| 3 |
Diversity of the clinical presentation of the MMR gene biallelic mutations
|
Bougeard, Gaëlle
|
|
2013
|
13 |
1 |
p. 131-135
|
artikel
|
| 4 |
Does and should breast cancer genetic counselling include lifestyle advice?
|
Albada, Akke
|
|
2013
|
13 |
1 |
p. 35-44
|
artikel
|
| 5 |
Endometrial tumour BRAF mutations and MLH1 promoter methylation as predictors of germline mismatch repair gene mutation status: a literature review
|
Metcalf, Alexander M.
|
|
2013
|
13 |
1 |
p. 1-12
|
artikel
|
| 6 |
Genetic variation at 8q24, family history of cancer, and upper gastrointestinal cancers in a Chinese population
|
Tarleton, Heather P.
|
|
2013
|
13 |
1 |
p. 45-56
|
artikel
|
| 7 |
Illness perceptions, risk perception and worry in SDH mutation carriers
|
Hulsteijn, L. T. van
|
|
2013
|
13 |
1 |
p. 83-91
|
artikel
|
| 8 |
Impact of breast cancer family history on tumor detection and tumor size in women newly-diagnosed with invasive breast cancer
|
Schwab, Fabienne Dominique
|
|
2013
|
13 |
1 |
p. 99-107
|
artikel
|
| 9 |
Lack of association between let-7 binding site polymorphism rs712 and risk of nasopharyngeal carcinoma
|
Pan, Xin-Min
|
|
2013
|
13 |
1 |
p. 93-97
|
artikel
|
| 10 |
Lynch Syndrome in high risk Ashkenazi Jews in Israel
|
Goldberg, Yael
|
|
2013
|
13 |
1 |
p. 65-73
|
artikel
|
| 11 |
Mammographic surveillance in women aged 35–39 at enhanced familial risk of breast cancer (FH02)
|
Evans, D. G.
|
|
2013
|
13 |
1 |
p. 13-21
|
artikel
|
| 12 |
MAX mutations status in Swedish patients with pheochromocytoma and paraganglioma tumours
|
Crona, Joakim
|
|
2013
|
13 |
1 |
p. 121-125
|
artikel
|
| 13 |
No evidence of genetic anticipation in a large family with Lynch syndrome
|
Stupart, D.
|
|
2013
|
13 |
1 |
p. 29-34
|
artikel
|
| 14 |
Reflex testing for Lynch syndrome: If we build it, will they come? Lessons learned from the uptake of clinical genetics services by individuals with newly diagnosed colorectal cancer (CRC)
|
Tomiak, E.
|
|
2013
|
13 |
1 |
p. 75-82
|
artikel
|
| 15 |
The MDM2 285G–309G haplotype is associated with an earlier age of tumour onset in patients with Li-Fraumeni syndrome
|
Renaux-Petel, Mariette
|
|
2013
|
13 |
1 |
p. 127-130
|
artikel
|
| 16 |
The prevalence of small intestinal polyps in patients with familial adenomatous polyposis: a prospective capsule endoscopy study
|
Yamada, Atsuo
|
|
2013
|
13 |
1 |
p. 23-28
|
artikel
|
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