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Familial Cancer|March 16, 2012
The evolution of personalized cancer genetic counseling in the era of personalized medicineHetal S Vig, Catharine Wang
Familial Cancer|December 20, 2019
The (ir)relevance of the abandoned criterion II for the diagnosis of serrated polyposis syndrome: a retrospective cohort studyArne G C Bleijenberg, Joep E G IJspeert, Daniel Rodríguez-Alcalde, et al.
Familial Cancer|December 21, 2019
De novo pathogenic germline variant in PALB2 in a patient with pancreatic cancerRinat Bernstein Molho, Shelly Zalmanoviz, Yael Laitman, et al.
Familial Cancer|March 16, 2020
Lack of evidence for CDK12 as an ovarian cancer predisposing geneAlexandre Eeckhoutte, Mathilde Saint-Ghislain, Manon Reverdy, et al.
Familial Cancer|January 29, 2019
Moving into the mainstream: healthcare professionals' views of implementing treatment focussed genetic testing in breast cancer careNina Hallowell, S Wright, D Stirling, et al.
Familial Cancer|November 2, 2019
Clear cell chondrosarcoma in Von Hippel-Lindau diseaseKoen M A Dreijerink, Rachel S van Leeuwaarde, Wenzel M Hackeng, et al.
Familial Cancer|November 28, 2019
'We don't know for sure': discussion of uncertainty concerning multigene panel testing during initial cancer genetic consultationsNiki M Medendorp, Marij A Hillen, Pomme E A van Maarschalkerweerd, et al.
Familial Cancer|February 13, 2020
Missense PALB2 germline variant disrupts nuclear localization of PALB2 in a patient with breast cancerMing Ren Toh, Chen Ee Low, Siao Ting Chong, et al.
Familial Cancer|February 8, 2019
Implementation of a Systematic Tumor Screening Program for Lynch Syndrome in an Integrated Health Care SettingElizabeth V Clarke, Kristin R Muessig, Jamilyn Zepp, et al.
Familial Cancer|November 28, 2018
Hereditary brain tumor with a homozygous germline mutation in PMS2: pedigree analysis and prenatal screening in a family with constitutional mismatch repair deficiency (CMMRD) syndromeShahid Mahmood Baig, Ambrin Fatima, Muhammad Tariq, et al.
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