| no |
title |
author |
magazine |
year |
volume |
issue |
page(s) |
type |
| 1 |
Age at diagnosis of cancer in 185delAG BRCA1 mutation carriers of diverse ethnicities: tentative evidence for modifier factors
|
Laitman, Yael
|
|
|
20 |
3 |
p. 189-194
|
article
|
| 2 |
A novel germline variant in RET gene resulting in an additional cysteine in a family with familial medullary thyroid carcinoma
|
Oriola, Josep
|
|
|
20 |
3 |
p. 253-256
|
article
|
| 3 |
Discordant DNA mismatch repair protein status between synchronous or metachronous gastrointestinal carcinomas: frequency, patterns, and molecular etiologies
|
Vyas, Monika
|
|
|
20 |
3 |
p. 201-213
|
article
|
| 4 |
Early-onset malignant phyllodes breast tumor in a patient with germline pathogenic variants in NF1 and BRCA1 genes
|
Gensini, Francesca
|
|
|
20 |
3 |
p. 195-199
|
article
|
| 5 |
Efficacy of paired tumor and germline testing in evaluation of patients with Lynch-like syndrome in a large integrated healthcare setting
|
Carwana, Holly
|
|
|
20 |
3 |
p. 223-230
|
article
|
| 6 |
FRAMe: Familial Risk Assessment of Melanoma—a risk prediction tool to guide CDKN2A germline mutation testing in Australian familial melanoma
|
Holland, Elizabeth A.
|
|
|
20 |
3 |
p. 231-239
|
article
|
| 7 |
Frequency and spectrum of mutations across 94 cancer predisposition genes in African American women with invasive breast cancer
|
Lovejoy, Leann A.
|
|
|
20 |
3 |
p. 181-187
|
article
|
| 8 |
Hereditary medullary thyroid carcinoma syndromes: experience from western India
|
Diwaker, Chakra
|
|
|
20 |
3 |
p. 241-251
|
article
|
| 9 |
Identification and management of Lynch syndrome in the Middle East and North African countries: outcome of a survey in 12 countries
|
Sina, Mohammad
|
|
|
20 |
3 |
p. 215-221
|
article
|
| 10 |
In memoriam Professor Thierry Frébourg
|
Bougeard, Gaëlle
|
|
|
20 |
3 |
p. 171-172
|
article
|
| 11 |
The role of TP53 pathogenic variants in early-onset HER2-positive breast cancer
|
Escudeiro, Carla
|
|
|
20 |
3 |
p. 173-180
|
article
|
Journal description