| nr |
titel |
auteur |
tijdschrift |
jaar |
jaarg. |
afl. |
pagina('s) |
type |
| 1 |
A lesson from a reported pathogenic variant in Peutz-Jeghers syndrome: a case report
|
Tan, Hu
|
|
2017
|
16 |
3 |
p. 417-422
|
artikel
|
| 2 |
ATM mutations for surgeons
|
Mansfield, Sara A.
|
|
2016
|
16 |
3 |
p. 407-410
|
artikel
|
| 3 |
Baseline results from the UK SIGNIFY study: a whole-body MRI screening study in TP53 mutation carriers and matched controls
|
Saya, Sibel
|
|
2017
|
16 |
3 |
p. 433-440
|
artikel
|
| 4 |
Biallelic BRCA2 mutations in two black South African children with Fanconi anaemia
|
Feben, Candice
|
|
2017
|
16 |
3 |
p. 441-446
|
artikel
|
| 5 |
Correlation between germline mutations in MMR genes and microsatellite instability in ovarian cancer specimens
|
Akbari, Mohammad R.
|
|
2017
|
16 |
3 |
p. 351-355
|
artikel
|
| 6 |
Detection of false positive mutations in BRCA gene by next generation sequencing
|
Suryavanshi, Moushumi
|
|
2016
|
16 |
3 |
p. 311-317
|
artikel
|
| 7 |
Embryonal rhabdomyosarcoma in a patient with a heterozygous frameshift variant in the DICER1 gene and additional manifestations of the DICER1 syndrome
|
Fremerey, Julia
|
|
2016
|
16 |
3 |
p. 401-405
|
artikel
|
| 8 |
Gastric cancer in FAP: a concerning rise in incidence
|
Mankaney, Gautam
|
|
2017
|
16 |
3 |
p. 371-376
|
artikel
|
| 9 |
Gastric tumours in FAP
|
Walton, Sarah-Jane
|
|
2017
|
16 |
3 |
p. 363-369
|
artikel
|
| 10 |
Identification of a rare germline NBN gene mutation by whole exome sequencing in a lung-cancer survivor from a large family with various types of cancer
|
Marafie, Makia J.
|
|
2016
|
16 |
3 |
p. 389-394
|
artikel
|
| 11 |
Identification of MSH2 inversion of exons 1–7 in clinical evaluation of families with suspected Lynch syndrome
|
Mork, Maureen E.
|
|
2016
|
16 |
3 |
p. 357-361
|
artikel
|
| 12 |
Mutation screening of ACKR3 and COPS8 in kidney cancer cases from the CONFIRM study
|
Mahmoodi, Maryam
|
|
2016
|
16 |
3 |
p. 411-416
|
artikel
|
| 13 |
Novel and reported pathogenic variants in exon 11 of BRCA2 gene in a cohort of Sri Lankan young breast cancer patients
|
Silva, Sumadee De
|
|
2016
|
16 |
3 |
p. 329-338
|
artikel
|
| 14 |
Outcomes of retesting BRCA negative patients using multigene panels
|
Yadav, Siddhartha
|
|
2016
|
16 |
3 |
p. 319-328
|
artikel
|
| 15 |
Patients with negative multi-gene panel testing: a back to the future paradox?
|
Sorscher, Steven M.
|
|
2017
|
16 |
3 |
p. 459
|
artikel
|
| 16 |
Psychosocial morbidity in TP53 mutation carriers: is whole-body cancer screening beneficial?
|
McBride, Kate A.
|
|
2017
|
16 |
3 |
p. 423-432
|
artikel
|
| 17 |
Supporting disclosure of genetic information to family members: professional practice and timelines in cancer genetics
|
Derbez, Benjamin
|
|
2017
|
16 |
3 |
p. 447-457
|
artikel
|
| 18 |
The association between prognosis of breast cancer and first-degree family history of breast or ovarian cancer: a systematic review and meta-analysis
|
Song, Jun-Long
|
|
2017
|
16 |
3 |
p. 339-349
|
artikel
|
| 19 |
The hereditary nature of small cell carcinoma of the ovary, hypercalcemic type: two new familial cases
|
Witkowski, Leora
|
|
2016
|
16 |
3 |
p. 395-399
|
artikel
|
| 20 |
Universal screening for Lynch syndrome among patients with colorectal cancer: patient perspectives on screening and sharing results with at-risk relatives
|
Hunter, Jessica Ezzell
|
|
2017
|
16 |
3 |
p. 377-387
|
artikel
|
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