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                             33 gevonden resultaten
nr titel auteur tijdschrift jaar jaarg. afl. pagina('s) type
1 A distinct mutation on the alternative splice site of APC exon 9 results in attenuated familial adenomatous polyposis phenotype Fostira, Florentia
2009
9 3 p. 395-400
artikel
2 Analysis of mismatch repair gene mutations in Turkish HNPCC patients Tunca, Berrin
2010
9 3 p. 365-376
artikel
3 A new familial cancer syndrome including predisposition to Wilms tumor and neuroblastoma Abbaszadeh, Fatemeh
2010
9 3 p. 425-430
artikel
4 Assessment of clinical practices among cancer genetic counselors Wham, Deborah
2010
9 3 p. 459-468
artikel
5 Atypical identification of Lynch syndrome by immunohistochemistry and microsatellite instability analysis on jejunal adenocarcinoma McIlvried, D. E.
2010
9 3 p. 377-381
artikel
6 Cancer family history characterization in an unselected cohort of 121 patients with uveal melanoma Abdel-Rahman, M. H.
2010
9 3 p. 431-438
artikel
7 Can self-esteem, mastery and perceived stigma predict long-term adjustment in women carrying a BRCA1/2-mutation? Evidence from a multi-center study Vodermaier, Andrea
2010
9 3 p. 305-311
artikel
8 Carney triad versus Carney Stratakis syndrome: two cases which illustrate the difficulty in distinguishing between these conditions in individual patients Alrashdi, Ismail
2010
9 3 p. 443-447
artikel
9 Detection of allelic imbalance in MLH1 expression by pyrosequencing serves as a tool for the identification of germline defects in Lynch syndrome Kwok, Chau-To
2010
9 3 p. 345-356
artikel
10 Differences in clinical and pathological characteristics of colorectal cancer in Arab as compared to Jewish patients in Northern Israel Glushko, Yelena
2010
9 3 p. 327-330
artikel
11 Erratum to: Survey of familial glioma and role of germline p16INK4A/p14ARF and p53 mutation Robertson, Lindsay B.
2010
9 3 p. 423-424
artikel
12 Familial adenomatous polyposis (FAP) and gender. Does gender influence the genetic transmission of FAP? Farinella, Eriberto
2010
9 3 p. 405-406
artikel
13 High risk for neoplastic transformation of endometriosis in a carrier of lynch syndrome Nyiraneza, Christine
2010
9 3 p. 383-387
artikel
14 Identification of a Danish breast/ovarian cancer family double heterozygote for BRCA1 and BRCA2 mutations Steffensen, Ane Y.
2010
9 3 p. 283-287
artikel
15 Identification of the first case of germline duplication of BRCA1 exon 13 in an Italian family Cerutti, Roberta
2009
9 3 p. 275-282
artikel
16 “I have always believed I was at high risk…” The role of expectation in emotional responses to the receipt of an average, moderate or high cancer genetic risk assessment result: a thematic analysis of free-text questionnaire comments Hilgart, J.
2010
9 3 p. 469-477
artikel
17 Juvenile nasopharyngeal angiofibroma: no evidence for inheritance or association with familial adenomatous polyposis Klockars, Tuomas
2010
9 3 p. 401-403
artikel
18 Knowledge, attitudes, and clinical experience of physicians regarding preimplantation genetic diagnosis for hereditary cancer predisposition syndromes Brandt, Amanda C.
2010
9 3 p. 479-487
artikel
19 Location in the large bowel influences the APC mutations observed in FAP adenomas Will, O. C.
2010
9 3 p. 389-393
artikel
20 LOH analysis should not be used as a tool to assess whether UVs of BRCA1/2 are pathogenic or not Beristain, E.
2010
9 3 p. 289-290
artikel
21 Lynch syndrome: the influence of environmental factors on extracolonic cancer risk in hMLH1 c.C1528T mutation carriers and their mutation-negative sisters Blokhuis, M. M.
2010
9 3 p. 357-363
artikel
22 Novel germline mutations in BRCA2 gene among breast and breast-ovarian cancer families from Poland Balabas, Aneta
2010
9 3 p. 267-274
artikel
23 Novel one-stop multidisciplinary follow-up clinic significantly improves cancer risk management in BRCA1/2 carriers Pichert, G.
2010
9 3 p. 313-319
artikel
24 Pregnancy after prophylactic total gastrectomy Kaurah, Pardeep
2010
9 3 p. 331-334
artikel
25 Prevalence of BRCA2 and CDKN2a mutations in German familial pancreatic cancer families Slater, Emily P.
2010
9 3 p. 335-343
artikel
26 RASSF1A polymorphism in familial breast cancer Bergqvist, J.
2010
9 3 p. 263-265
artikel
27 Relationship of BRCA1 and BRCA2 mutations with cancer burden in the family and tumor incidence Esteban Cardeñosa, Eva
2010
9 3 p. 291-295
artikel
28 Screening for germline DND1 mutations in testicular cancer patients Sijmons, Rolf H.
2010
9 3 p. 439-442
artikel
29 Successful oxytocin-assisted nipple aspiration in women at increased risk for breast cancer Suijkerbuijk, Karijn P. M.
2010
9 3 p. 321-325
artikel
30 Surgical prophylaxis in familial adenomatous polyposis: do pre-existing desmoids outside the abdominal cavity matter? Sinha, Ashish
2010
9 3 p. 407-411
artikel
31 Survey of familial glioma and role of germline p16INK4A/p14ARF and p53 mutation Robertson, Lindsay B.
2010
9 3 p. 413-421
artikel
32 Update multiple endocrine neoplasia type 2 Raue, Friedhelm
2010
9 3 p. 449-457
artikel
33 Uptake of predictive testing among relatives of BRCA1 and BRCA2 families: a multicenter study in northeastern Spain Sanz, Judit
2009
9 3 p. 297-304
artikel
                             33 gevonden resultaten
 
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