| nr |
titel |
auteur |
tijdschrift |
jaar |
jaarg. |
afl. |
pagina('s) |
type |
| 1 |
A case of contralateral breast cancer and skin cancer associated with NBN heterozygous pathogenic variant c.698_701delAACA
|
Gass, Jennifer
|
|
2017
|
16 |
4 |
p. 551-553
|
artikel
|
| 2 |
All in the family? Communication of cancer survivors with their families
|
Bowen, Deborah J.
|
|
2017
|
16 |
4 |
p. 597-603
|
artikel
|
| 3 |
A new POT1 germline mutation—expanding the spectrum of POT1-associated cancers
|
Wilson, Tremika Le-Shan
|
|
2017
|
16 |
4 |
p. 561-566
|
artikel
|
| 4 |
A novel TP53 germline inframe deletion identified in a Spanish series of Li-fraumeni syndrome suspected families
|
Llovet, Patricia
|
|
2017
|
16 |
4 |
p. 567-575
|
artikel
|
| 5 |
A Peutz–Jeghers syndrome family associated with sinonasal adenocarcinoma: 28 years follow up report
|
Chiang, Jy-Ming
|
|
2017
|
16 |
4 |
p. 555-560
|
artikel
|
| 6 |
Elucidating the clinical significance of two PMS2 missense variants coexisting in a family fulfilling hereditary cancer criteria
|
González-Acosta, Maribel
|
|
2017
|
16 |
4 |
p. 501-507
|
artikel
|
| 7 |
General practitioner attitudes towards prescribing aspirin to carriers of Lynch Syndrome: findings from a national survey
|
Smith, Samuel G.
|
|
2017
|
16 |
4 |
p. 509-516
|
artikel
|
| 8 |
Genetic polymorphisms of NFκB1-94ins/delATTG and NFκBIA-881A/G genes in Egyptian patients with colorectal cancer
|
Youssef, Mohamed Ragab
|
|
2017
|
16 |
4 |
p. 517-524
|
artikel
|
| 9 |
High-risk individuals’ perceptions of reproductive genetic testing for CDH1 mutations
|
Hallowell, Nina
|
|
2017
|
16 |
4 |
p. 531-535
|
artikel
|
| 10 |
Identification of novel potential genetic predictors of urothelial bladder carcinoma susceptibility in Pakistani population
|
Ali, Syeda Hafiza Benish
|
|
2017
|
16 |
4 |
p. 577-594
|
artikel
|
| 11 |
Importance of updating family cancer history in childhood cancer survivors
|
Russo, Selena
|
|
2017
|
16 |
4 |
p. 605-610
|
artikel
|
| 12 |
Improved quality of risk-reducing salpingo-oophorectomy in Australasian women at high risk of pelvic serous cancer
|
Lee, Y. C.
|
|
2017
|
16 |
4 |
p. 461-469
|
artikel
|
| 13 |
Inherited DNA repair gene mutations detected by tumor next generation sequencing in urinary tract cancers
|
Gupta, Sumati
|
|
2017
|
16 |
4 |
p. 545-550
|
artikel
|
| 14 |
Loss of MSH2 and MSH6 due to heterozygous germline defects in MSH3 and MSH6
|
Morak, Monika
|
|
2017
|
16 |
4 |
p. 491-500
|
artikel
|
| 15 |
Lower gastrointestinal neuroendocrine neoplasms associated with hereditary cancer syndromes: a case series
|
Kidambi, Trilokesh D.
|
|
2017
|
16 |
4 |
p. 537-543
|
artikel
|
| 16 |
Molecular characterization and clinical interpretation of BRCA1/BRCA2 variants in families from Murcia (south-eastern Spain) with hereditary breast and ovarian cancer: clinical–pathological features in BRCA carriers and non-carriers
|
Gabaldó Barrios, Xavier
|
|
2017
|
16 |
4 |
p. 477-489
|
artikel
|
| 17 |
Placing negative multi-gene panel results into clinical context
|
Hermel, David J.
|
|
2017
|
16 |
4 |
p. 595
|
artikel
|
| 18 |
Power of pedigree likelihood analysis in extended pedigrees to classify rare variants of uncertain significance in cancer risk genes
|
Rosenthal, Elisabeth A.
|
|
2017
|
16 |
4 |
p. 611-620
|
artikel
|
| 19 |
Prevalence of two BRCA1 mutations, 5382insC and 300T > G, in ovarian cancer patients from Ukraine
|
Gorodetska, I.
|
|
2017
|
16 |
4 |
p. 471-476
|
artikel
|
| 20 |
Universal screening for microsatellite instability in colorectal cancer in the clinical genomics era: new recommendations, methods, and considerations
|
Hechtman, Jaclyn F.
|
|
2017
|
16 |
4 |
p. 525-529
|
artikel
|
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