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                             12 gevonden resultaten
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
                             12 gevonden resultaten
 
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