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 |