| no |
title |
author |
magazine |
year |
volume |
issue |
page(s) |
type |
| 1 |
A novel pathogenic MLH1 missense mutation, c.112A > C, p.Asn38His, in six families with Lynch syndrome
|
van Riel, Els
|
|
2010
|
8 |
1 |
|
article
|
| 2 |
BRCA1 mutations in women with familial or early-onset breast cancer and BRCA2 mutations in familial cancer in Estonia
|
Tamboom, Kristiina
|
|
2010
|
8 |
1 |
|
article
|
| 3 |
Cancer and Lhermitte-Duclos disease are common in Cowden syndrome patients
|
Riegert-Johnson, Douglas L
|
|
2010
|
8 |
1 |
|
article
|
| 4 |
High penetrances of BRCA1 and BRCA2 mutations confirmed in a prospective series
|
Møller, Pål
|
|
2010
|
8 |
1 |
|
article
|
| 5 |
Is no news good news? Inconclusive genetic test results in BRCA1 and BRCA2 from patients and professionals' perspectives
|
Ardern-Jones, Audrey
|
|
2010
|
8 |
1 |
|
article
|
| 6 |
MSH6 and PMS2 mutation positive Australian Lynch syndrome families: novel mutations, cancer risk and age of diagnosis of colorectal cancer
|
Talseth-Palmer, Bente A
|
|
2010
|
8 |
1 |
|
article
|
| 7 |
Population screening for hereditary and familial cancer syndromes in Valka district of Latvia
|
Vanags, Andrejs
|
|
2010
|
8 |
1 |
|
article
|
| 8 |
Surveillance of FAP: a prospective blinded comparison of capsule endoscopy and other GI imaging to detect small bowel polyps
|
Tescher, Paul
|
|
2010
|
8 |
1 |
|
article
|
| 9 |
The revised Bethesda guidelines: extent of utilization in a university hospital medical center with a cancer genetics program
|
Mukherjee, Aparna
|
|
2010
|
8 |
1 |
|
article
|
Journal description