Analysis of patient reports on the referral process to two NSW cancer genetic services Grace I. Butel-SimoesAllan D. Spigelman Original Article 20 March 2014 Pages: 333 - 343
“Would you test your children without their consent?” and other sticky dilemmas in the field of cancer genetic testing Karina L. BrierleyDanielle C. BonadiesEllen T. Matloff Original Article 08 May 2014 Pages: 345 - 350
Limited diagnostic value of microsatellite instability associated pathology features in colorectal cancer Paul G. van PuttenMargot G. F. van LierJ. Han van Krieken Original Article 18 March 2014 Pages: 351 - 359
Two Chinese pedigrees for adenomatous polyposis coli: new mutations at codon 1309 and predisposition to phenotypic variations Dai-Xiang LiaoBing LiCheng-Hua Luo Short Communication 25 March 2014 Pages: 361 - 368
Fertility and apparent genetic anticipation in Lynch syndrome Douglas StupartAung Ko WinRajkumar Ramesar Original Article 28 March 2014 Pages: 369 - 374
An unusual case of familial adenomatous polyposis with very early symptom occurrence Maurizio Ponz de LeonMaria Anastasia BianchiniAlfredo Cacciari Original Article 26 April 2014 Pages: 375 - 380
Evaluating the utilization of educational materials in communicating about Lynch syndrome to at-risk relatives Kristen DilzellKerry KinghamUri Ladabaum Original Article 27 April 2014 Pages: 381 - 389
How harmful is genetic testing for familial adenomatous polyposis (FAP) in young children; the parents’ experience Anna A. Kattentidt-MouravievaM. den HeijerA. Wagner Original Article 17 May 2014 Pages: 391 - 399
A founder MLH1 mutation in Lynch syndrome families from Piedmont, Italy, is associated with an increased risk of pancreatic tumours and diverse immunohistochemical patterns Iolanda BorelliGuido C. Casalis CavalchiniBarbara Pasini Original Article 07 May 2014 Pages: 401 - 413
Nucleotide variants of the cancer predisposing gene CDH1 and the risk of non-syndromic cleft lip with or without cleft palate Kamil K. HozyaszAdrianna MostowskaPaweł P. Jagodziński Original Article Open access 17 May 2014 Pages: 415 - 421
Attitudes and compliance of clinical management after genetic testing for hereditary breast and ovarian cancer among high-risk Southern Chinese females with breast cancer history Ava KwongAnnie Tsz-Wai ChuDesiree Man-Sik Tse Original Article 13 March 2014 Pages: 423 - 430
Novel BRCA1 deleterious mutation (c.1918C>T) in familial breast and ovarian cancer syndrome who share a common ancestry Xavier Gabaldó BarriosMaría Desamparados Sarabia MeseguerFrancisco Ruiz Espejo Short Communication 16 March 2014 Pages: 431 - 435
BRCA1 point mutations in premenopausal breast cancer patients from Central Sudan Ida BiunnoGitana AcetoRenato Mariani-Costantini Original Article 12 April 2014 Pages: 437 - 444
BRCA1 founder mutations compared to ovarian cancer in Belarus Alena SavanevichOleg OszurekJacek Gronwald Short Communication Open access 27 April 2014 Pages: 445 - 447
Duplex value of caveolin-1 in non-small cell lung cancer: a meta analysis Dali ChenCheng ShenGuowei Che Review 08 March 2014 Pages: 449 - 457
Mosaic partial deletion of the PTEN gene in a patient with Cowden syndrome Erin E. Salo-MullenJinru ShiaZsofia K. Stadler Original Article 08 March 2014 Pages: 459 - 467
A family history questionnaire improves detection of women at risk for hereditary gynecologic cancer: a pilot study Margot M. KoenemanArnold-Jan KruseRoy F. P. M. Kruitwagen Original Article 15 March 2014 Pages: 469 - 475
Intronic splicing mutations in PTCH1 cause Gorlin syndrome Zaynab BholahMiriam J. SmithWilliam G. Newman Short Communication 22 March 2014 Pages: 477 - 480
Influence of family history on psychosocial distress and perceived need for treatment in prostate cancer survivors Andreas DinkelMarielouise KornmayerKathleen Herkommer Original Article 09 April 2014 Pages: 481 - 488
A survey of the practice patterns of gynecologic oncologists dealing with hereditary cancer patients in Japan Noriko TanabeAyumi ShikamaChikako Shimizu Original Article 23 May 2014 Pages: 489 - 498
Genetics of endometrial cancer Ayelet ShaiYakir SegevSteven A. Narod Review Article 17 May 2014 Pages: 499 - 505
Exploring the association of succinate dehydrogenase complex mutations with lymphoid malignancies R. RenellaJ. CarnevaleK. A. Janeway Short Communication 30 April 2014 Pages: 507 - 511
Erratum to: Frequency of 5382insC mutation of BRCA1 gene among breast cancer patients: an experience from Eastern India Abhijit ChakrabortyAshis MukhopadhyayJayasri Basak Erratum 14 June 2014 Pages: 513 - 513