no |
title |
author |
magazine |
year |
volume |
issue |
page(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 |
article |
2 |
Ameloblastoma: a neglected criterion for nevoid basal cell carcinoma (Gorlin) syndrome
|
Ponti, Giovanni |
|
2012 |
11 |
3 |
p. 411-418 |
article |
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 |
article |
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 |
article |
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 |
article |
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 |
article |
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 |
article |
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 |
article |
9 |
Causes of death of mutation carriers in Finnish Lynch syndrome families
|
Pylvänäinen, Kirsi |
|
2012 |
11 |
3 |
p. 467-471 |
article |
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 |
article |
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 |
article |
12 |
Common MUTYH mutations and colorectal cancer risk in multiethnic populations
|
Lejbkowicz, Flavio |
|
2012 |
11 |
3 |
p. 329-335 |
article |
13 |
Familial gastric cancer: guidelines for diagnosis, treatment and periodic surveillance
|
Kluijt, Irma |
|
2012 |
11 |
3 |
p. 363-369 |
article |
14 |
French experts report on MUTYH-associated polyposis (MAP)
|
Buecher, Bruno |
|
2012 |
11 |
3 |
p. 321-328 |
article |
15 |
Germline mutations in BRIP1 and PALB2 in Jewish high cancer risk families
|
Catucci, Irene |
|
2012 |
11 |
3 |
p. 483-491 |
article |
16 |
Hepatoblastoma in two siblings and familial adenomatous polyposis: causal nexus or coincidence?
|
Evers, Christina |
|
2012 |
11 |
3 |
p. 529-533 |
article |
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 |
article |
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 |
article |
19 |
Microsatellite instability testing in Korean patients with colorectal cancer
|
Oh, Jung Ryul |
|
2012 |
11 |
3 |
p. 459-466 |
article |
20 |
Molecular characterization of parathyroid tumors from two patients with hereditary colorectal cancer syndromes
|
Andreasson, Adam |
|
2012 |
11 |
3 |
p. 355-362 |
article |
21 |
Mutation screening of RAD51C in high-risk breast and ovarian cancer families
|
Lu, Wenping |
|
2012 |
11 |
3 |
p. 381-385 |
article |
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 |
article |
23 |
Novel germline c-MET mutation in a family with hereditary papillary renal carcinoma
|
Wadt, Karin A. W. |
|
2012 |
11 |
3 |
p. 535-537 |
article |
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 |
article |
25 |
Q48P mutation in the hMLH1 gene associated with Lynch syndrome in three Hungarian families
|
Tanyi, Miklós |
|
2012 |
11 |
3 |
p. 519-524 |
article |
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 |
article |
27 |
The evolution of personalized cancer genetic counseling in the era of personalized medicine
|
Vig, Hetal S. |
|
2012 |
11 |
3 |
p. 539-544 |
article |
28 |
The IL-10 promoter haplotype and cancer risk: evidence from a meta-analysis
|
Zhang, Kui |
|
2012 |
11 |
3 |
p. 313-319 |
article |
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 |
article |
30 |
Uroepithelial and kidney carcinoma in Lynch syndrome
|
Aarnio, Markku |
|
2012 |
11 |
3 |
p. 395-401 |
article |