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Familial Cancer|July 31, 2021
Unusual phenotypes in patients with a pathogenic germline variant in DICER1Kateryna Venger, Miriam Elbracht, Julia Carlens, et al.
Familial Cancer|July 5, 2022
A case of Rothmund-Thomson syndrome originally thought to be a case of Bloom syndromeDavid Humberto Marmolejo Castañeda, Mara Cruellas Lapeña, Estela Carrasco López, et al.
Familial Cancer|June 19, 2022
Potential risks associated with the use of ionizing radiation for imaging and treatment of colorectal cancer in Lynch syndrome patientsMingzhu Sun, Jayne Moquet, Michele Ellender, et al.
Familial Cancer|June 22, 2022
Universal tumor screening for lynch syndrome on colorectal cancer biopsies impacts surgical treatment decisionsJennifer Vazzano, Jewel Tomlinson, Peter P Stanich, et al.
Familial Cancer|May 31, 2021
Review of guidelines for the identification and clinical care of patients with genetic predisposition for hematological malignanciesBrigitte Schlegelberger, Cristina Mecucci, Marcin Wlodarski
Familial Cancer|June 24, 2017
The role of screening MRI in the era of next generation sequencing and moderate-risk genetic mutationsSarah Macklin, Jennifer Gass, Ghada Mitri, et al.
Familial Cancer|September 15, 2016
Hereditary breast and ovarian cancer: successful systematic implementation of a group approach to genetic counsellingPatrick R Benusiglio, Marina Di Maria, Leila Dorling, et al.
Familial Cancer|October 22, 2021
Medullary thyroid cancer and pheochromocytoma in MEN2A: are there parent of origin effects on disease expression?Andreas Machens, Kerstin Lorenz, Frank Weber, et al.
Familial Cancer|October 12, 2021
Familial colorectal cancer and tooth agenesis caused by an AXIN2 variant: how do we detect families with rare cancer predisposition syndromes?Janni M Jensen, Anne Skakkebæk, Mette Gaustadness, et al.
Familial Cancer|July 22, 2022
Remote vs in-person BRCA1/2 non-carriers test disclosure: patients' choice during Covid-19 pandemic restrictionSilvia Costanzo, Simona De Summa, Leonarda Maurmo, et al.
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