| no |
title |
author |
magazine |
year |
volume |
issue |
page(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
|
article
|
| 2 |
Analysis of mismatch repair gene mutations in Turkish HNPCC patients
|
Tunca, Berrin
|
|
2010
|
9 |
3 |
p. 365-376
|
article
|
| 3 |
A new familial cancer syndrome including predisposition to Wilms tumor and neuroblastoma
|
Abbaszadeh, Fatemeh
|
|
2010
|
9 |
3 |
p. 425-430
|
article
|
| 4 |
Assessment of clinical practices among cancer genetic counselors
|
Wham, Deborah
|
|
2010
|
9 |
3 |
p. 459-468
|
article
|
| 5 |
Atypical identification of Lynch syndrome by immunohistochemistry and microsatellite instability analysis on jejunal adenocarcinoma
|
McIlvried, D. E.
|
|
2010
|
9 |
3 |
p. 377-381
|
article
|
| 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
|
article
|
| 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
|
article
|
| 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
|
article
|
| 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
|
article
|
| 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
|
article
|
| 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
|
article
|
| 12 |
Familial adenomatous polyposis (FAP) and gender. Does gender influence the genetic transmission of FAP?
|
Farinella, Eriberto
|
|
2010
|
9 |
3 |
p. 405-406
|
article
|
| 13 |
High risk for neoplastic transformation of endometriosis in a carrier of lynch syndrome
|
Nyiraneza, Christine
|
|
2010
|
9 |
3 |
p. 383-387
|
article
|
| 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
|
article
|
| 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
|
article
|
| 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
|
article
|
| 17 |
Juvenile nasopharyngeal angiofibroma: no evidence for inheritance or association with familial adenomatous polyposis
|
Klockars, Tuomas
|
|
2010
|
9 |
3 |
p. 401-403
|
article
|
| 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
|
article
|
| 19 |
Location in the large bowel influences the APC mutations observed in FAP adenomas
|
Will, O. C.
|
|
2010
|
9 |
3 |
p. 389-393
|
article
|
| 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
|
article
|
| 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
|
article
|
| 22 |
Novel germline mutations in BRCA2 gene among breast and breast-ovarian cancer families from Poland
|
Balabas, Aneta
|
|
2010
|
9 |
3 |
p. 267-274
|
article
|
| 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
|
article
|
| 24 |
Pregnancy after prophylactic total gastrectomy
|
Kaurah, Pardeep
|
|
2010
|
9 |
3 |
p. 331-334
|
article
|
| 25 |
Prevalence of BRCA2 and CDKN2a mutations in German familial pancreatic cancer families
|
Slater, Emily P.
|
|
2010
|
9 |
3 |
p. 335-343
|
article
|
| 26 |
RASSF1A polymorphism in familial breast cancer
|
Bergqvist, J.
|
|
2010
|
9 |
3 |
p. 263-265
|
article
|
| 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
|
article
|
| 28 |
Screening for germline DND1 mutations in testicular cancer patients
|
Sijmons, Rolf H.
|
|
2010
|
9 |
3 |
p. 439-442
|
article
|
| 29 |
Successful oxytocin-assisted nipple aspiration in women at increased risk for breast cancer
|
Suijkerbuijk, Karijn P. M.
|
|
2010
|
9 |
3 |
p. 321-325
|
article
|
| 30 |
Surgical prophylaxis in familial adenomatous polyposis: do pre-existing desmoids outside the abdominal cavity matter?
|
Sinha, Ashish
|
|
2010
|
9 |
3 |
p. 407-411
|
article
|
| 31 |
Survey of familial glioma and role of germline p16INK4A/p14ARF and p53 mutation
|
Robertson, Lindsay B.
|
|
2010
|
9 |
3 |
p. 413-421
|
article
|
| 32 |
Update multiple endocrine neoplasia type 2
|
Raue, Friedhelm
|
|
2010
|
9 |
3 |
p. 449-457
|
article
|
| 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
|
article
|
Journal description