nr |
titel |
auteur |
tijdschrift |
jaar |
jaarg. |
afl. |
pagina('s) |
type |
1 |
Analysis of uveal melanomas and paired constitutional DNA for exclusion of a BAP1-tumor predisposition syndrome
|
Abbassi, Yasaman Arjmand |
|
|
22 |
2 |
p. 193-202 |
artikel |
2 |
A need to tailor surveillance based on family history: describing a highly penetrant familial paraganglioma kindred with an SDHD pathogenic variant
|
Foley, Madeline |
|
|
22 |
2 |
p. 217-224 |
artikel |
3 |
A pilot study investigating feasibility of mainstreaming germline BRCA1 and BRCA2 testing in high-risk patients with breast and/or ovarian cancer in three tertiary Cancer Centres in Ireland
|
McVeigh, Terri Patricia |
|
|
22 |
2 |
p. 135-149 |
artikel |
4 |
Barriers to completion of cascade genetic testing: how can we improve the uptake of testing for hereditary breast and ovarian cancer syndrome?
|
Kahn, Ryan Matthew |
|
|
22 |
2 |
p. 127-133 |
artikel |
5 |
CDH1 mutations recurrence and global clustering in genetically tested families with hereditary diffuse gastric cancer syndrome: results from a systematic study
|
Corso, Giovanni |
|
|
22 |
2 |
p. 187-192 |
artikel |
6 |
2022 CGA-IGC Annual Meeting: The collaborative group of the Americas on Inherited Gastrointestinal Cancer November 11–13, 2022
|
|
|
|
22 |
2 |
p. 237-282 |
artikel |
7 |
Characterization of sebaceous and non-sebaceous cutaneous manifestations in patients with lynch syndrome: a systematic review
|
Aziz, Shahram |
|
|
22 |
2 |
p. 167-175 |
artikel |
8 |
Determinants of adherence to recommendations on physical activity, red and processed meat intake, and body weight among lynch syndrome patients
|
Hoedjes, M |
|
|
22 |
2 |
p. 155-166 |
artikel |
9 |
Disclosure of genetic risk to dating partners among young adults with von Hippel-Lindau disease
|
Bond, Elysa |
|
|
22 |
2 |
p. 203-215 |
artikel |
10 |
Identifying the BRCA1 c.-107A > T variant in Dutch patients with a tumor BRCA1 promoter hypermethylation
|
de Jong, Vincent M. T. |
|
|
22 |
2 |
p. 151-154 |
artikel |
11 |
Laboratory variation in the grading of dysplasia of duodenal adenomas in familial adenomatous polyposis patients
|
Soons, E. |
|
|
22 |
2 |
p. 177-186 |
artikel |
12 |
Next-generation universal hereditary cancer screening: implementation of an automated hereditary cancer screening program for patients with advanced cancer undergoing tumor sequencing in a large HMO
|
Hoffman, Trevor L. |
|
|
22 |
2 |
p. 225-235 |
artikel |