| nr |
titel |
auteur |
tijdschrift |
jaar |
jaarg. |
afl. |
pagina('s) |
type |
| 1 |
A squamous cell carcinoma in a young woman with Lynch syndrome
|
Adan, F.
|
|
2018
|
18 |
2 |
p. 193-196
|
artikel
|
| 2 |
Boosting care and knowledge about hereditary cancer: European Reference Network on Genetic Tumour Risk Syndromes
|
Vos, Janet R.
|
|
2018
|
18 |
2 |
p. 281-284
|
artikel
|
| 3 |
Cleft lip/palate and hereditary diffuse gastric cancer: report of a family harboring a CDH1 c.687 + 1G > A germline mutation and review of the literature
|
Obermair, Florian
|
|
2018
|
18 |
2 |
p. 253-260
|
artikel
|
| 4 |
Development and pilot testing of a leaflet informing women with breast cancer about genomic testing for polygenic risk
|
Kaur, Rajneesh
|
|
2018
|
18 |
2 |
p. 147-152
|
artikel
|
| 5 |
Electronically ascertained extended pedigrees in breast cancer genetic counseling
|
Stefansdottir, V.
|
|
2018
|
18 |
2 |
p. 153-160
|
artikel
|
| 6 |
Exploring the preferences of involved health professionals regarding the implementation of an online decision aid to support couples during reproductive decision-making in hereditary cancer: a mixed methods approach
|
Reumkens, Kelly
|
|
2019
|
18 |
2 |
p. 285-291
|
artikel
|
| 7 |
Genetic counselling of young women with breast cancer for Li–Fraumeni syndrome: a nationwide survey on the experiences and attitudes of genetics professionals
|
Bakhuizen, J. J.
|
|
2018
|
18 |
2 |
p. 231-239
|
artikel
|
| 8 |
Germline mutation p.N363K in POLE is associated with an increased risk of colorectal cancer and giant cell glioblastoma
|
Vande Perre, P.
|
|
2018
|
18 |
2 |
p. 173-178
|
artikel
|
| 9 |
Hereditary brain tumor with a homozygous germline mutation in PMS2: pedigree analysis and prenatal screening in a family with constitutional mismatch repair deficiency (CMMRD) syndrome
|
Baig, Shahid Mahmood
|
|
2018
|
18 |
2 |
p. 261-265
|
artikel
|
| 10 |
Interest in, willingness-to-pay for and willingness-to-recommend genetic testing for prostate cancer among affected men after radical prostatectomy
|
Mayer, Marcel
|
|
2018
|
18 |
2 |
p. 221-230
|
artikel
|
| 11 |
Massive juvenile polyposis of the stomach in a family with SMAD4 gene mutation
|
Leon, Maurizio Ponz de
|
|
2018
|
18 |
2 |
p. 165-172
|
artikel
|
| 12 |
Monoallelic MUTYH carrier status is not associated with increased breast cancer risk in a multigene panel cohort
|
Fulk, Kelly
|
|
2018
|
18 |
2 |
p. 197-201
|
artikel
|
| 13 |
Multi-gene panel testing confirms phenotypic variability in MUTYH-Associated Polyposis
|
Sutcliffe, Erin G.
|
|
2019
|
18 |
2 |
p. 203-209
|
artikel
|
| 14 |
NTHL1-associate polyposis: first Australian case report
|
Groves, Alexandra
|
|
2019
|
18 |
2 |
p. 179-182
|
artikel
|
| 15 |
Ovarian small cell carcinoma in one of a pair of monozygous twins
|
Fahiminiya, Somayyeh
|
|
2018
|
18 |
2 |
p. 161-163
|
artikel
|
| 16 |
Progress report on the major clinical advances in patient-oriented research into familial melanoma (2013–2018)
|
Visser, Mijke
|
|
2019
|
18 |
2 |
p. 267-271
|
artikel
|
| 17 |
Recent advances in Lynch syndrome
|
Biller, Leah H.
|
|
2019
|
18 |
2 |
p. 211-219
|
artikel
|
| 18 |
Referral frequency, attrition rate, and outcomes of germline testing in patients with pancreatic adenocarcinoma
|
Walker, Evan J.
|
|
2018
|
18 |
2 |
p. 241-251
|
artikel
|
| 19 |
Risk of multiple colorectal cancer development depends on age and subgroup in individuals with hereditary predisposition
|
Lindberg, Lars J.
|
|
2018
|
18 |
2 |
p. 183-191
|
artikel
|
| 20 |
TP53 germline mutation testing in early-onset breast cancer: findings from a nationwide cohort
|
Bakhuizen, J. J.
|
|
2019
|
18 |
2 |
p. 273-280
|
artikel
|
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