| nr |
titel |
auteur |
tijdschrift |
jaar |
jaarg. |
afl. |
pagina('s) |
type |
| 1 |
Abstracts of the 4th meeting of the European Hereditary Tumour Group, Barcelona, Spain, October 17–19th, 2019
|
|
|
|
19 |
1 |
p. 77-121
|
artikel
|
| 2 |
A unique case of two somatic APC mutations in an early onset cribriform-morular variant of papillary thyroid carcinoma and overview of the literature
|
Aydemirli, M. D.
|
|
|
19 |
1 |
p. 15-21
|
artikel
|
| 3 |
Clear cell chondrosarcoma in Von Hippel-Lindau disease
|
Dreijerink, Koen M. A.
|
|
|
19 |
1 |
p. 41-45
|
artikel
|
| 4 |
Long-term positive psychological outcomes in an Australian pancreatic cancer screening program
|
O’Neill, R. S.
|
|
|
19 |
1 |
p. 23-35
|
artikel
|
| 5 |
MLH1 promoter hypermethylation: are you absolutely sure about the absence of MLH1 germline mutation? About a new case
|
Kientz, Caroline
|
|
|
19 |
1 |
p. 11-14
|
artikel
|
| 6 |
Neurofibromatosis type 2 discordance in monozygous twins
|
Amico, S.
|
|
|
19 |
1 |
p. 37-40
|
artikel
|
| 7 |
Novel candidates in early-onset familial colorectal cancer
|
Jansen, Anne M. L.
|
|
|
19 |
1 |
p. 1-10
|
artikel
|
| 8 |
Radiotherapy-induced malignancies in breast cancer patients with TP53 pathogenic germline variants (Li–Fraumeni syndrome)
|
Petry, Vanessa
|
|
|
19 |
1 |
p. 47-53
|
artikel
|
| 9 |
Renal cell carcinoma in young FH mutation carriers: case series and review of the literature
|
Hol, J. A.
|
|
|
19 |
1 |
p. 55-63
|
artikel
|
| 10 |
‘We don’t know for sure’: discussion of uncertainty concerning multigene panel testing during initial cancer genetic consultations
|
Medendorp, Niki M.
|
|
|
19 |
1 |
p. 65-76
|
artikel
|
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