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                             27 gevonden resultaten
nr titel auteur tijdschrift jaar jaarg. afl. pagina('s) type
1 A cost-effectiveness analysis of prophylactic surgery versus gynecologic surveillance for women from hereditary non-polyposis colorectal cancer (HNPCC) Families Yang, Kathleen Y.
2011
10 3 p. 535-543
artikel
2 Adequacy of risk-reducing gynaecologic surgery in BRCA1 or BRCA2 mutation carriers and other women at high risk of pelvic serous cancer Kiely, B. E.
2011
10 3 p. 505-514
artikel
3 A novel pathogenic germline mutation in the adenomatous polyposis coli gene in a Tunisian family with FAP Miladi-Abdennadher, Imen
2011
10 3 p. 567-571
artikel
4 A putative Lynch syndrome family carrying MSH2 and MSH6 variants of uncertain significance—functional analysis reveals the pathogenic one Kantelinen, Jukka
2011
10 3 p. 515-520
artikel
5 A rationale for mTOR inhibitors as chemoprevention agents in Peutz-Jeghers syndrome Kuwada, Scott K.
2011
10 3 p. 469-472
artikel
6 Attitudes toward childbearing and prenatal testing in individuals undergoing genetic testing for Lynch Syndrome Dewanwala, Akriti
2011
10 3 p. 549-556
artikel
7 Cancer worry among Norwegian male BRCA1/2 mutation carriers Strømsvik, Nina
2011
10 3 p. 597-603
artikel
8 Case studies in the diagnosis and management of Peutz-Jeghers syndrome Riegert-Johnson, Douglas
2011
10 3 p. 463-468
artikel
9 Dendritic cell and macrophage infiltration in microsatellite-unstable and microsatellite-stable colorectal cancer Bauer, Kathrin
2011
10 3 p. 557-565
artikel
10 Factors associated with an individuals’ decision to withdraw from genetic counseling for BRCA1 and BRCA2 genes mutations: are personality traits involved? Caruso, Anita
2011
10 3 p. 581-589
artikel
11 Familial breast cancer: is it time to move from a reactive to a proactive role? Harris, H.
2011
10 3 p. 501-503
artikel
12 Familial colorectal cancer: eleven years of data from a registry program in Switzerland Kovac, Michal
2011
10 3 p. 605-616
artikel
13 Gastrointestinal polyps and cancer in Peutz-Jeghers syndrome: clinical aspects Latchford, A. R.
2011
10 3 p. 455-461
artikel
14 Introduction Menko, Fred H.
2011
10 3 p. 413-414
artikel
15 Lack of germline PALB2 mutations in melanoma-prone families with CDKN2A mutations and pancreatic cancer Yang, Xiaohong R.
2011
10 3 p. 545-548
artikel
16 LKB1 as the ghostwriter of crypt history Jansen, Marnix
2011
10 3 p. 437-446
artikel
17 LKB1 signaling in advancing cell differentiation Udd, Lina
2011
10 3 p. 425-435
artikel
18 Low penetrance hereditary retinoblastoma in a family: what should we consider in the genetic counselling process and follow up? Serrano, C.
2011
10 3 p. 617-621
artikel
19 Malignant fibrous histiocytoma is a rare Lynch syndrome-associated tumor in two German families Brieger, Angela
2011
10 3 p. 591-595
artikel
20 Management of renal tumors in Von Hippel-Lindau disease by percutaneous CT fluoroscopic guided radiofrequency ablation: preliminary results Iwamoto, Yoichi
2011
10 3 p. 529-534
artikel
21 Peutz-Jeghers syndrome: a patient’s view Sugars, Stephanie
2011
10 3 p. 473-479
artikel
22 Progression of duodenal adenomatosis in familial adenomatous polyposis: due to ageing of subjects and advances in technology Mathus-Vliegen, Elisabeth M. H.
2011
10 3 p. 491-499
artikel
23 Serum levels of IGF-I and BRCA penetrance: a case control study in breast cancer families Pasanisi, Patrizia
2011
10 3 p. 521-528
artikel
24 The differential diagnosis of familial lentiginosis syndromes Lodish, Maya B.
2011
10 3 p. 481-490
artikel
25 The LKB1 complex-AMPK pathway: the tree that hides the forest Sebbagh, Michaël
2011
10 3 p. 415-424
artikel
26 The role of LKB1 in lung cancer Sanchez-Cespedes, Montse
2011
10 3 p. 447-453
artikel
27 The sex ratio and age of onset features of gastric cancer patients in hereditary diffuse gastric cancer families Yu, Junxiu
2011
10 3 p. 573-579
artikel
                             27 gevonden resultaten
 
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