RASSF1A polymorphism in familial breast cancer J. BergqvistA. LatifW. G. Newman BriefCommunication 02 April 2010 Pages: 263 - 265
Novel germline mutations in BRCA2 gene among breast and breast-ovarian cancer families from Poland Aneta BalabasElzbieta SkaskoPawel Blecharz OriginalPaper 10 April 2010 Pages: 267 - 274
Identification of the first case of germline duplication of BRCA1 exon 13 in an Italian family Roberta CeruttiNora SahnaneCarlo Capella BriefCommunication 30 December 2009 Pages: 275 - 282
Identification of a Danish breast/ovarian cancer family double heterozygote for BRCA1 and BRCA2 mutations Ane Y. SteffensenLars JønsonThomas V. O. Hansen OriginalPaper Open access 09 May 2010 Pages: 283 - 287
LOH analysis should not be used as a tool to assess whether UVs of BRCA1/2 are pathogenic or not E. BeristainI. GuerraM. I. Tejada Letter 07 January 2010 Pages: 289 - 290
Relationship of BRCA1 and BRCA2 mutations with cancer burden in the family and tumor incidence Eva Esteban CardeñosaPascual Bolufer GilabertOn behalf of the Group for Assessment for Hereditary Cancer of Valencian Community OriginalPaper 21 February 2010 Pages: 291 - 295
Uptake of predictive testing among relatives of BRCA1 and BRCA2 families: a multicenter study in northeastern Spain Judit SanzTeresa Ramón y CajalJudith Balmaña OriginalPaper 20 December 2009 Pages: 297 - 304
Can self-esteem, mastery and perceived stigma predict long-term adjustment in women carrying a BRCA1/2-mutation? Evidence from a multi-center study Andrea VodermaierMary Jane EsplenChristine Maheu OriginalPaper 06 February 2010 Pages: 305 - 311
Novel one-stop multidisciplinary follow-up clinic significantly improves cancer risk management in BRCA1/2 carriers G. PichertC. JacobsL. Izatt OriginalPaper 19 March 2010 Pages: 313 - 319
Successful oxytocin-assisted nipple aspiration in women at increased risk for breast cancer Karijn P. M. SuijkerbuijkElsken van der WallPaul J. van Diest BriefCommunication Open access 05 May 2010 Pages: 321 - 325
Differences in clinical and pathological characteristics of colorectal cancer in Arab as compared to Jewish patients in Northern Israel Yelena GlushkoWalid BasherJamal Zidan OriginalPaper 16 April 2010 Pages: 327 - 330
Pregnancy after prophylactic total gastrectomy Pardeep KaurahRebecca FitzgeraldDavid G. Huntsman OriginalPaper 09 January 2010 Pages: 331 - 334
Prevalence of BRCA2 and CDKN2a mutations in German familial pancreatic cancer families Emily P. SlaterPeter LangerDetlef K. Bartsch OriginalPaper 27 February 2010 Pages: 335 - 343
Detection of allelic imbalance in MLH1 expression by pyrosequencing serves as a tool for the identification of germline defects in Lynch syndrome Chau-To KwokRobyn L. WardMegan P. Hitchins OriginalPaper 09 January 2010 Pages: 345 - 356
Lynch syndrome: the influence of environmental factors on extracolonic cancer risk in hMLH1 c.C1528T mutation carriers and their mutation-negative sisters M. M. BlokhuisG. E. PietersenR. S. Ramesar OriginalPaper 17 July 2010 Pages: 357 - 363
Analysis of mismatch repair gene mutations in Turkish HNPCC patients Berrin TuncaMonica PedroniMaurizio Ponz de Leon OriginalPaper 06 April 2010 Pages: 365 - 376
Atypical identification of Lynch syndrome by immunohistochemistry and microsatellite instability analysis on jejunal adenocarcinoma D. E. McIlvriedR. E. BirhirayJ. Z. Lu OriginalPaper 09 April 2010 Pages: 377 - 381
High risk for neoplastic transformation of endometriosis in a carrier of lynch syndrome Christine NyiranezaEtienne MarbaixKarin Dahan OriginalPaper 20 January 2010 Pages: 383 - 387
Location in the large bowel influences the APC mutations observed in FAP adenomas O. C. WillS. J. LeedhamI. P. M. Tomlinson OriginalPaper 13 March 2010 Pages: 389 - 393
A distinct mutation on the alternative splice site of APC exon 9 results in attenuated familial adenomatous polyposis phenotype Florentia FostiraDrakoulis Yannoukakos BriefCommunication 24 December 2009 Pages: 395 - 400
Juvenile nasopharyngeal angiofibroma: no evidence for inheritance or association with familial adenomatous polyposis Tuomas KlockarsSuvi RenkonenAntti A. Mäkitie BriefCommunication 13 March 2010 Pages: 401 - 403
Familial adenomatous polyposis (FAP) and gender. Does gender influence the genetic transmission of FAP? Eriberto FarinellaRamawad SoobrahSusan K. Clark OriginalPaper 22 April 2010 Pages: 405 - 406
Surgical prophylaxis in familial adenomatous polyposis: do pre-existing desmoids outside the abdominal cavity matter? Ashish SinhaDaniel C. GibbonsSue Clark OriginalPaper 29 April 2010 Pages: 407 - 411
Survey of familial glioma and role of germline p16 INK4A /p14 ARF and p53 mutation Lindsay B. RobertsonGeorgina N. ArmstrongRichard S. Houlston OriginalPaper 09 May 2010 Pages: 413 - 421
Erratum to: Survey of familial glioma and role of germline p16 INK4A /p14 ARF and p53 mutation Lindsay B. RobertsonGeorgina N. ArmstrongRichard S. Houlston Erratum 09 June 2010 Pages: 423 - 424
A new familial cancer syndrome including predisposition to Wilms tumor and neuroblastoma Fatemeh AbbaszadehKaren T. BarkerNazneen Rahman OriginalPaper 07 January 2010 Pages: 425 - 430
Cancer family history characterization in an unselected cohort of 121 patients with uveal melanoma M. H. Abdel-RahmanR. PilarskiF. H. Davidorf OriginalPaper 16 February 2010 Pages: 431 - 438
Screening for germline DND1 mutations in testicular cancer patients Rolf H. SijmonsYvonne J. VosHarald J. Hoekstra OriginalPaper Open access 22 April 2010 Pages: 439 - 442
Carney triad versus Carney Stratakis syndrome: two cases which illustrate the difficulty in distinguishing between these conditions in individual patients Ismail AlrashdiGul BanoShirley V. Hodgson OriginalPaper 30 January 2010 Pages: 443 - 447
Update multiple endocrine neoplasia type 2 Friedhelm RaueKarin Frank-Raue OriginalPaper 20 January 2010 Pages: 449 - 457
Assessment of clinical practices among cancer genetic counselors Deborah WhamThuy VuBrandie Heald OriginalPaper 06 February 2010 Pages: 459 - 468
“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 J. HilgartC. PhelpsA. Murray OriginalPaper 30 January 2010 Pages: 469 - 477
Knowledge, attitudes, and clinical experience of physicians regarding preimplantation genetic diagnosis for hereditary cancer predisposition syndromes Amanda C. BrandtMatthew L. TschirgiKaren H. Lu OriginalPaper 30 April 2010 Pages: 479 - 487
