| nr |
titel |
auteur |
tijdschrift |
jaar |
jaarg. |
afl. |
pagina('s) |
type |
| 1 |
Abstracts
|
|
|
2013
|
12 |
3 |
p. 405-448
|
artikel
|
| 2 |
A case of pneumatosis cystoides intestinalis mimicking familial adenomatous polyposis
|
Ponz de Leon, Maurizio
|
|
2012
|
12 |
3 |
p. 573-576
|
artikel
|
| 3 |
A complex endocrine conundrum
|
Bano, G.
|
|
2012
|
12 |
3 |
p. 577-580
|
artikel
|
| 4 |
A de novoFLCN mutation in a patient with spontaneous pneumothorax and renal cancer; a clinical and molecular evaluation
|
Menko, Fred H.
|
|
2012
|
12 |
3 |
p. 373-379
|
artikel
|
| 5 |
Birt–Hogg–Dubé syndrome
|
Czyzyk-Krzeska, Maria F.
|
|
2013
|
12 |
3 |
p. 355-356
|
artikel
|
| 6 |
Birt–Hogg–Dubé syndrome and the skin
|
Vernooij, Marigje
|
|
2013
|
12 |
3 |
p. 381-385
|
artikel
|
| 7 |
Birt–Hogg–Dubé syndrome: from gene discovery to molecularly targeted therapies
|
Schmidt, Laura S.
|
|
2012
|
12 |
3 |
p. 357-364
|
artikel
|
| 8 |
Birt–Hogg–Dubé: tumour suppressor function and signalling dynamics central to folliculin
|
Tee, Andrew R.
|
|
2012
|
12 |
3 |
p. 367-372
|
artikel
|
| 9 |
Body image issues after bilateral prophylactic mastectomy with breast reconstruction in healthy women at risk for hereditary breast cancer
|
Gopie, Jessica P.
|
|
2012
|
12 |
3 |
p. 479-487
|
artikel
|
| 10 |
Cancer family history triage: a key step in the decision to offer screening and genetic testing
|
Brennan, Paul
|
|
2012
|
12 |
3 |
p. 497-502
|
artikel
|
| 11 |
Clinical characterization and mutation spectrum in Hispanic families with adenomatous polyposis syndromes
|
Cruz-Correa, Marcia
|
|
2013
|
12 |
3 |
p. 555-562
|
artikel
|
| 12 |
Detection of large deletions in the VHL gene using a Real-Time PCR with SYBR Green
|
Ebenazer, Andrew
|
|
2013
|
12 |
3 |
p. 519-524
|
artikel
|
| 13 |
Detection of large scale 3′ deletions in the PMS2 gene amongst Colon-CFR participants: have we been missing anything?
|
Clendenning, Mark
|
|
2013
|
12 |
3 |
p. 563-566
|
artikel
|
| 14 |
Diagnosis and management of BHD-associated kidney cancer
|
Stamatakis, Lambros
|
|
2013
|
12 |
3 |
p. 397-402
|
artikel
|
| 15 |
Erratum to: Birt–Hogg–Dubé: beyond the clinical manifestations
|
Middelton, Lindsay A.
|
|
2013
|
12 |
3 |
p. 403
|
artikel
|
| 16 |
Erratum to: Birt–Hogg–Dubé syndrome: from gene discovery to molecularly targeted therapies
|
Schmidt, Laura S.
|
|
2013
|
12 |
3 |
p. 365
|
artikel
|
| 17 |
Erratum to: Closing the loop: an interactive action research conference format for delivering updated medical information while eliciting Latina patient/family experiences and psychosocial needs post-genetic cancer risk assessment
|
MacDonald, Deborah J.
|
|
2013
|
12 |
3 |
p. 585
|
artikel
|
| 18 |
Erratum to: Evaluating Lynch syndrome in very early onset colorectal cancer probands without apparent polyposis
|
Jasperson, Kory W.
|
|
2013
|
12 |
3 |
p. 583
|
artikel
|
| 19 |
Familial adenomatous polyposis: not all masses are desmoids
|
Sloane, J.
|
|
2013
|
12 |
3 |
p. 525-528
|
artikel
|
| 20 |
Frequency of 5382insC mutation of BRCA1 gene among breast cancer patients: an experience from Eastern India
|
Chakraborty, Abhijit
|
|
2012
|
12 |
3 |
p. 489-495
|
artikel
|
| 21 |
GNAS is not involved in gastrointestinal tumour formation in Peutz-Jeghers syndrome
|
Korsse, Susanne E.
|
|
2013
|
12 |
3 |
p. 581-582
|
artikel
|
| 22 |
Mutation screen and RNA analysis disclose the changed splicing of the E-cadherin transcription in gastric cancer
|
Li, Xiaowei
|
|
2013
|
12 |
3 |
p. 547-554
|
artikel
|
| 23 |
Mutation screening in a Norwegian cohort with pheochromocytoma
|
Sjursen, Wenche
|
|
2013
|
12 |
3 |
p. 529-535
|
artikel
|
| 24 |
Preparing individuals to communicate genetic test results to their relatives: report of a randomized control trial
|
Montgomery, Susan V.
|
|
2013
|
12 |
3 |
p. 537-546
|
artikel
|
| 25 |
Pulmonary manifestations of Birt-Hogg-Dubé syndrome
|
Gupta, Nishant
|
|
2013
|
12 |
3 |
p. 387-396
|
artikel
|
| 26 |
Screening participation for people at increased risk of colorectal cancer due to family history: a systematic review and meta-analysis
|
Ait Ouakrim, Driss
|
|
2013
|
12 |
3 |
p. 459-472
|
artikel
|
| 27 |
Searching for E-cadherin gene mutations in early onset diffuse gastric cancer and hereditary diffuse gastric cancer in Korean patients
|
Kim, Sollip
|
|
2012
|
12 |
3 |
p. 503-507
|
artikel
|
| 28 |
Splice site mutations in mismatch repair genes and risk of cancer in the general population
|
Thomsen, Mette
|
|
2013
|
12 |
3 |
p. 567-572
|
artikel
|
| 29 |
The prognostic value of MGMT promoter methylation in Glioblastoma multiforme: a meta-analysis
|
Zhang, Kui
|
|
2013
|
12 |
3 |
p. 449-458
|
artikel
|
| 30 |
The risk of gastric cancer in carriers of CHEK2 mutations
|
Teodorczyk, Urszula
|
|
2013
|
12 |
3 |
p. 473-478
|
artikel
|
| 31 |
Unmet support needs and distress among women with a BRCA1/2 mutation
|
Farrelly, Ashley
|
|
2012
|
12 |
3 |
p. 509-518
|
artikel
|
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