| nr |
titel |
auteur |
tijdschrift |
jaar |
jaarg. |
afl. |
pagina('s) |
type |
| 1 |
Aortopulmonary window parathyroid gland causing primary hyperparathyroidism in men type 1 syndrome
|
Tonelli, Francesco
|
|
2015
|
15 |
1 |
p. 133-138
|
artikel
|
| 2 |
Association between the FTOrs8050136 polymorphism and cancer risk: a meta-analysis
|
Zhao, Jian
|
|
2015
|
15 |
1 |
p. 145-153
|
artikel
|
| 3 |
Association of APC I1307K and E1317Q polymorphisms with colorectal cancer among Egyptian subjects
|
Abdel-Malak, Camelia
|
|
2015
|
15 |
1 |
p. 49-56
|
artikel
|
| 4 |
Birt–Hogg–Dubé syndrome: novel FLCN frameshift deletion in daughter and father with renal cell carcinomas
|
Näf, Ernst
|
|
2015
|
15 |
1 |
p. 127-132
|
artikel
|
| 5 |
Contribution of APC and MUTYH mutations to familial adenomatous polyposis susceptibility in Hungary
|
Papp, Janos
|
|
2015
|
15 |
1 |
p. 85-97
|
artikel
|
| 6 |
First report of somatic mosaicism for mutations in STK11 in four patients with Peutz–Jeghers syndrome
|
McKay, Victoria
|
|
2015
|
15 |
1 |
p. 57-61
|
artikel
|
| 7 |
Genetic testing for Lynch syndrome: family communication and motivation
|
Leenen, Celine H. M.
|
|
2015
|
15 |
1 |
p. 63-73
|
artikel
|
| 8 |
Germline TERT promoter mutations are rare in familial melanoma
|
Harland, Mark
|
|
2015
|
15 |
1 |
p. 139-144
|
artikel
|
| 9 |
Incidental diagnosis of HLRCC following investigation for Asperger Syndrome: actionable and actioned
|
Duong, Bich-Thu
|
|
2015
|
15 |
1 |
p. 25-29
|
artikel
|
| 10 |
Is there an association between invasive lobular carcinoma of the breast and a family history of gastric cancer?
|
Chikman, Bar
|
|
2015
|
15 |
1 |
p. 41-47
|
artikel
|
| 11 |
Long-term outcome of sporadic and FAP-associated desmoid tumors treated with high-dose selective estrogen receptor modulators and sulindac: a single-center long-term observational study in 134 patients
|
Quast, Daniel Robert
|
|
2015
|
15 |
1 |
p. 31-40
|
artikel
|
| 12 |
Ovarian tumors related to intronic mutations in DICER1: a report from the international ovarian and testicular stromal tumor registry
|
Schultz, Kris Ann P.
|
|
2015
|
15 |
1 |
p. 105-110
|
artikel
|
| 13 |
Rhabdoid tumor predisposition syndrome caused by SMARCB1 constitutional deletion: prenatal detection of new case of recurrence in siblings due to gonadal mosaicism
|
Gigante, Laura
|
|
2015
|
15 |
1 |
p. 123-126
|
artikel
|
| 14 |
Screening of HELQ in breast and ovarian cancer families
|
Pelttari, Liisa M.
|
|
2015
|
15 |
1 |
p. 19-23
|
artikel
|
| 15 |
Screening of RET gene mutations in Chinese patients with medullary thyroid carcinoma and their relatives
|
Wang, Junyi
|
|
2015
|
15 |
1 |
p. 99-104
|
artikel
|
| 16 |
Surveillance using capsule endoscopy is safe in post-colectomy patients with familial adenomatous polyposis: a prospective Japanese study
|
Matsumoto, Minori
|
|
2015
|
15 |
1 |
p. 75-83
|
artikel
|
| 17 |
The knowledge value-chain of genetic counseling for breast cancer: an empirical assessment of prediction and communication processes
|
Amara, Nabil
|
|
2015
|
15 |
1 |
p. 1-17
|
artikel
|
| 18 |
The role of germline mutations in the BRCA1/2 and mismatch repair genes in men ascertained for early-onset and/or familial prostate cancer
|
Maia, Sofia
|
|
2015
|
15 |
1 |
p. 111-121
|
artikel
|
Tijdschrift beschrijving