| nr |
titel |
auteur |
tijdschrift |
jaar |
jaarg. |
afl. |
pagina('s) |
type |
| 1 |
A model for patient-direct screening and referral for familial cancer risk
|
Niendorf, Kristin B.
|
|
2016
|
15 |
4 |
p. 707-716
|
artikel
|
| 2 |
A mutation of the succinate dehydrogenase B gene in a Korean family with paraganglioma
|
Sagong, Borum
|
|
2016
|
15 |
4 |
p. 601-606
|
artikel
|
| 3 |
Angelina and Brad effect
|
Eisinger, Francois
|
|
2016
|
15 |
4 |
p. 541-542
|
artikel
|
| 4 |
An investigation of the factors effecting high-risk individuals’ decision-making about prophylactic total gastrectomy and surveillance for hereditary diffuse gastric cancer (HDGC)
|
Hallowell, Nina
|
|
2016
|
15 |
4 |
p. 665-676
|
artikel
|
| 5 |
BRCA1/BRCA2 founder mutations and cancer risks: impact in the western Danish population
|
Nielsen, Henriette Roed
|
|
2016
|
15 |
4 |
p. 507-512
|
artikel
|
| 6 |
Colorectal cancer risk variants at 8q23.3 and 11q23.1 are associated with disease phenotype in APC mutation carriers
|
Ghorbanoghli, Z.
|
|
2016
|
15 |
4 |
p. 563-570
|
artikel
|
| 7 |
Communicating genetic test results within the family: Is it lost in translation? A survey of relatives in the randomized six-step study
|
Daly, Mary B.
|
|
2016
|
15 |
4 |
p. 697-706
|
artikel
|
| 8 |
CTNNB1-mutant colorectal carcinomas with immediate invasive growth: a model of interval cancers in Lynch syndrome
|
Ahadova, Aysel
|
|
2016
|
15 |
4 |
p. 579-586
|
artikel
|
| 9 |
Decentralized colonoscopic surveillance with high patient compliance prevents hereditary and familial colorectal cancer
|
Sjöström, Olle
|
|
2016
|
15 |
4 |
p. 543-551
|
artikel
|
| 10 |
Difference in CXCR4 expression between sporadic and VHL-related hemangioblastoma
|
Kruizinga, Roeliene C.
|
|
2016
|
15 |
4 |
p. 607-616
|
artikel
|
| 11 |
Evaluation of laboratory perspectives on hereditary cancer panels
|
Stoll, Jessica
|
|
2016
|
15 |
4 |
p. 689-696
|
artikel
|
| 12 |
Evaluation of TP53 Pro72Arg and MDM2 SNP285–SNP309 polymorphisms in an Italian cohort of LFS suggestive patients lacking identifiable TP53 germline mutations
|
Ponti, Francesca
|
|
2016
|
15 |
4 |
p. 635-643
|
artikel
|
| 13 |
Identification of a novel PMS2 alteration c.505C>G (R169G) in trans with a PMS2 pathogenic mutation in a patient with constitutional mismatch repair deficiency
|
Mork, Maureen E.
|
|
2016
|
15 |
4 |
p. 587-591
|
artikel
|
| 14 |
Increased incidence of bladder cancer, lymphoid leukaemia, and myeloma in a cohort of Queensland melanoma families
|
Read, Jazlyn
|
|
2016
|
15 |
4 |
p. 651-663
|
artikel
|
| 15 |
MEN 2A-related cutaneous lichen amyloidosis: report of three kindred and systematic literature review of clinical, biochemical and molecular characteristics
|
Scapineli, Jessica Oliboni
|
|
2016
|
15 |
4 |
p. 625-633
|
artikel
|
| 16 |
Modeling the dyadic effects of parenting, stress, and coping on parent–child communication in families tested for hereditary breast-ovarian cancer risk
|
Hamilton, Jada G.
|
|
2016
|
15 |
4 |
p. 513-522
|
artikel
|
| 17 |
MSI detection and its pitfalls in CMMRD syndrome in a family with a bi-allelic MLH1 mutation
|
Nguyen, Aurélia
|
|
2016
|
15 |
4 |
p. 571-577
|
artikel
|
| 18 |
Multiple endocrine neoplasia type 1 syndrome: single centre experience from western India
|
Goroshi, Manjunath
|
|
2016
|
15 |
4 |
p. 617-624
|
artikel
|
| 19 |
No evidence of increased breast cancer risk for proven noncarriers from BRCA1 and BRCA2 families
|
Nielsen, Henriette Roed
|
|
2016
|
15 |
4 |
p. 523-528
|
artikel
|
| 20 |
Occurrence of renal cell carcinoma and hematologic malignancies (predominantly lymphoid) in individuals and in families
|
Dutcher, Janice P.
|
|
2016
|
15 |
4 |
p. 677-687
|
artikel
|
| 21 |
Ovarian cancer patients at high risk of BRCA mutation: the constitutional genetic characterization does not change prognosis
|
Sabatier, Renaud
|
|
2016
|
15 |
4 |
p. 497-506
|
artikel
|
| 22 |
Patient and genetic counselor perceptions of in-person versus telephone genetic counseling for hereditary breast/ovarian cancer
|
Jacobs, Aryana S.
|
|
2016
|
15 |
4 |
p. 529-539
|
artikel
|
| 23 |
Rapid detection of germline mutations for hereditary gastrointestinal polyposis/cancers using HaloPlex target enrichment and high-throughput sequencing technologies
|
Kohda, Masakazu
|
|
2016
|
15 |
4 |
p. 553-562
|
artikel
|
| 24 |
Undefined familial colorectal cancer and the role of pleiotropism in cancer susceptibility genes
|
Dobbins, Sara E.
|
|
2016
|
15 |
4 |
p. 593-599
|
artikel
|
| 25 |
Ventricular fibrillation resulting from electrolyte imbalance reveals vipoma in MEN1 syndrome
|
Cavalli, Tiziana
|
|
2016
|
15 |
4 |
p. 645-649
|
artikel
|
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