nr |
titel |
auteur |
tijdschrift |
jaar |
jaarg. |
afl. |
pagina('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 |
artikel |
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 |
artikel |
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 |
artikel |
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 |
artikel |
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 |
artikel |
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 |
artikel |
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 |
artikel |
8 |
Hereditary medullary thyroid carcinoma syndromes: experience from western India
|
Diwaker, Chakra |
|
|
20 |
3 |
p. 241-251 |
artikel |
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 |
artikel |
10 |
In memoriam Professor Thierry Frébourg
|
Bougeard, Gaëlle |
|
|
20 |
3 |
p. 171-172 |
artikel |
11 |
The role of TP53 pathogenic variants in early-onset HER2-positive breast cancer
|
Escudeiro, Carla |
|
|
20 |
3 |
p. 173-180 |
artikel |