| nr |
titel |
auteur |
tijdschrift |
jaar |
jaarg. |
afl. |
pagina('s) |
type |
| 1 |
Adequacy of family history taking in ovarian cancer patients: a population-based study
|
Altena, Anne M. van
|
|
2012
|
11 |
3 |
p. 343-349
|
artikel
|
| 2 |
Ameloblastoma: a neglected criterion for nevoid basal cell carcinoma (Gorlin) syndrome
|
Ponti, Giovanni
|
|
2012
|
11 |
3 |
p. 411-418
|
artikel
|
| 3 |
A multidisciplinary clinic for individualizing management of patients at increased risk for breast and gynecologic cancer
|
Engel, Natalie J.
|
|
2012
|
11 |
3 |
p. 419-427
|
artikel
|
| 4 |
Analysis of a Finnish family confirms RHBDF2 mutations as the underlying factor in tylosis with esophageal cancer
|
Saarinen, Silva
|
|
2012
|
11 |
3 |
p. 525-528
|
artikel
|
| 5 |
A prospective study of bowel preparation for colonoscopy with polyethylene glycol-electrolyte solution versus sodium phosphate in Lynch syndrome: a randomized trial
|
Vugt van Pinxteren, Maria W. J. van
|
|
2012
|
11 |
3 |
p. 337-341
|
artikel
|
| 6 |
Breast and ovarian cancer risk management in a French cohort of 158 women carrying a BRCA1 or BRCA2 germline mutation: patient choices and outcome
|
This, Pascale
|
|
2012
|
11 |
3 |
p. 473-482
|
artikel
|
| 7 |
Breast cancer risk factors differ between Asian and white women with BRCA1/2 mutations
|
Bruin, Monique A. de
|
|
2012
|
11 |
3 |
p. 429-439
|
artikel
|
| 8 |
Cancer spectrum in DNA mismatch repair gene mutation carriers: results from a hospital based Lynch syndrome registry
|
Pande, Mala
|
|
2012
|
11 |
3 |
p. 441-447
|
artikel
|
| 9 |
Causes of death of mutation carriers in Finnish Lynch syndrome families
|
Pylvänäinen, Kirsi
|
|
2012
|
11 |
3 |
p. 467-471
|
artikel
|
| 10 |
Clinical correlation and molecular evaluation confirm that the MLH1 p.Arg182Gly (c.544A>G) mutation is pathogenic and causes Lynch syndrome
|
Farrell, Michael P.
|
|
2012
|
11 |
3 |
p. 509-518
|
artikel
|
| 11 |
Closing the loop: an interactive action-research conference format for delivering updated medical information while eliciting Latina patient/family experiences and psychosocial needs post-genetic cancer risk assessment
|
MacDonald, Deborah J.
|
|
2012
|
11 |
3 |
p. 449-458
|
artikel
|
| 12 |
Common MUTYH mutations and colorectal cancer risk in multiethnic populations
|
Lejbkowicz, Flavio
|
|
2012
|
11 |
3 |
p. 329-335
|
artikel
|
| 13 |
Familial gastric cancer: guidelines for diagnosis, treatment and periodic surveillance
|
Kluijt, Irma
|
|
2012
|
11 |
3 |
p. 363-369
|
artikel
|
| 14 |
French experts report on MUTYH-associated polyposis (MAP)
|
Buecher, Bruno
|
|
2012
|
11 |
3 |
p. 321-328
|
artikel
|
| 15 |
Germline mutations in BRIP1 and PALB2 in Jewish high cancer risk families
|
Catucci, Irene
|
|
2012
|
11 |
3 |
p. 483-491
|
artikel
|
| 16 |
Hepatoblastoma in two siblings and familial adenomatous polyposis: causal nexus or coincidence?
|
Evers, Christina
|
|
2012
|
11 |
3 |
p. 529-533
|
artikel
|
| 17 |
High prevalence of the c.1227_1228dup (p.Glu410GlyfsX43) mutation in Tunisian families affected with MUTYH-associated-polyposis
|
Abdelmaksoud-Dammak, Rania
|
|
2012
|
11 |
3 |
p. 503-508
|
artikel
|
| 18 |
Limited significance of family history for presence of BRCA1 gene mutation in Polish breast and ovarian cancer cases
|
Brozek, Izabela
|
|
2012
|
11 |
3 |
p. 351-354
|
artikel
|
| 19 |
Microsatellite instability testing in Korean patients with colorectal cancer
|
Oh, Jung Ryul
|
|
2012
|
11 |
3 |
p. 459-466
|
artikel
|
| 20 |
Molecular characterization of parathyroid tumors from two patients with hereditary colorectal cancer syndromes
|
Andreasson, Adam
|
|
2012
|
11 |
3 |
p. 355-362
|
artikel
|
| 21 |
Mutation screening of RAD51C in high-risk breast and ovarian cancer families
|
Lu, Wenping
|
|
2012
|
11 |
3 |
p. 381-385
|
artikel
|
| 22 |
Nephron sparing surgery in von Hippel-Lindau associated renal cell carcinoma; clinicopathological long-term follow-up
|
Jilg, C. A.
|
|
2012
|
11 |
3 |
p. 387-394
|
artikel
|
| 23 |
Novel germline c-MET mutation in a family with hereditary papillary renal carcinoma
|
Wadt, Karin A. W.
|
|
2012
|
11 |
3 |
p. 535-537
|
artikel
|
| 24 |
Outcomes of a systems-level intervention offering breast cancer risk assessments to low-income underserved women
|
Mays, Darren
|
|
2012
|
11 |
3 |
p. 493-502
|
artikel
|
| 25 |
Q48P mutation in the hMLH1 gene associated with Lynch syndrome in three Hungarian families
|
Tanyi, Miklós
|
|
2012
|
11 |
3 |
p. 519-524
|
artikel
|
| 26 |
The consequences of risk reducing salpingo-oophorectomy: the case for a coordinated approach to long-term follow up post surgical menopause
|
Pezaro, Carmel
|
|
2012
|
11 |
3 |
p. 403-410
|
artikel
|
| 27 |
The evolution of personalized cancer genetic counseling in the era of personalized medicine
|
Vig, Hetal S.
|
|
2012
|
11 |
3 |
p. 539-544
|
artikel
|
| 28 |
The IL-10 promoter haplotype and cancer risk: evidence from a meta-analysis
|
Zhang, Kui
|
|
2012
|
11 |
3 |
p. 313-319
|
artikel
|
| 29 |
The use of telephone in genetic counseling versus in-person counseling: a randomized study on counselees’ outcome
|
Platten, Ulla
|
|
2012
|
11 |
3 |
p. 371-379
|
artikel
|
| 30 |
Uroepithelial and kidney carcinoma in Lynch syndrome
|
Aarnio, Markku
|
|
2012
|
11 |
3 |
p. 395-401
|
artikel
|
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