Daniela Barana

Incidence of non-colorectal/endometrial malignancies in individuals with Lynch syndrome: a retrospective cohort study

Silvia Negro, Francesco Celotto, Francesca Schiavi, Marco Scarpa et autres

it, us (code pays fourni par la source)

Comprehensive genetic and epigenetic characterization of Lynch‐like syndrome patients

Francesca Pirini, Luciano Calzari, Gianluca Tedaldi, Michela Tebaldi et autres

it (code pays fourni par la source)

Expanding Lynch Syndrome Spectrum: The Role of Non-Colorectal/Endometrial Malignancies and Implications for Universal Tumor Screening

Silvia Negro, Francesco Celotto, Francesca Schiavi, Isabella Mammi et autres

it, in (code pays fourni par la source)

ItaLynch: an ongoing Italian study to evaluate the feasibility of mainstreaming the diagnosis of Lynch syndrome in colorectal cancer patients

Alberto Puccini, Federica Grillo, Matteo Fassan, Sara Lonardi et autres

it, us (code pays fourni par la source)

Filling the gap: A thorough investigation for the genetic diagnosis of unsolved polyposis patients with monoallelic MUTYH pathogenic variants

Anastasia Dell’Elice, Giulia Cini, Mara Fornasarig, Franco Armelao et autres

it (code pays fourni par la source)

Definition and management of colorectal polyposis not associated with APC/MUTYH germline pathogenic variants: AIFEG consensus statement

Emanuele Damiano Luca Urso, Maurizio Ponz de Leòn, Marco Vitellaro, Guglielmo Niccolò Piozzi et autres

it (code pays fourni par la source)

Segregation analysis of the BRCA2 c.9227G>T variant in multiple families suggests a pathogenic role in breast and ovarian cancer predisposition

Simona Agata, Silvia Tognazzo, Elisa Alducci, Laura Matricardi et autres

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Whole‐exome sequencing and targeted gene sequencing provide insights into the role of PALB2 as a male breast cancer susceptibility gene

Valentina Silvestri, Veronica Zelli, Virginia Valentini, Piera Rizzolo et autres

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Style modification in breast and Colorectal Cancer Patients: results of a pilot study Long-Survivors

M Pegoraro, Daniela Barana, G. Schiavo, I. Fracca et autres

it (code pays fourni par la source)

MUTYH c.933+3A>C, associated with a severely impaired gene expression, is the first Italian founder mutation in MUTYH‐Associated Polyposis

Elisa Pin, Chiara Pastrello, Rossella Tricarico, Laura Papi et autres

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Characterization of the Most Frequent MUTYH Mutation C.933+3a>C (Ivs10+3a>C) in the Northeastern Italian Population

Elisa Pin, Michele Quaia, Rossella Tricarico, Alessandra Viel et autres

BRCA1 p.Val1688del Is a Deleterious Mutation That Recurs in Breast and Ovarian Cancer Families From Northeast Italy

Sandro Malacrida, Simona Agata, Monia Callegaro, Cinzia Casella et autres

it (code pays fourni par la source)