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Familial Cancer|October 24, 2020
Identification and management of Lynch syndrome in the Middle East and North African countries: outcome of a survey in 12 countriesMohammad Sina, Zeinab Ghorbanoghli, Amal Abedrabbo, et al.
Familial Cancer|January 31, 2020
Detection of DNA mismatch repair deficient crypts in random colonoscopic biopsies identifies Lynch syndrome patientsRandall E Brand, Beth Dudley, Eve Karloski, et al.
Familial Cancer|February 1, 2020
Prevalence of CNV-neutral structural genomic rearrangements in MLH1, MSH2, and PMS2 not detectable in routine NGS diagnosticsMonika Morak, Verena Steinke-Lange, Trisari Massdorf, et al.
Familial Cancer|June 2, 2022
Prevalence and risk factors of barrett's esophagus in lynch syndromeNatalie Farha, Ruishen Lyu, David Liska, et al.
Familial Cancer|November 27, 2022
A retrospective cohort study of genetic referral and diagnosis of Lynch syndrome in patients with cutaneous sebaceous lesionsMeera Kattapuram, Christina Shabet, Sarah Austin, et al.
Familial Cancer|May 22, 2019
Endoscopic full thickness resection for early colon cancer in Lynch syndromeAlexandra M J Langers, Jurjen J Boonstra, James C H Hardwick, et al.
Familial Cancer|October 8, 2021
Re-evaluating cancer risks associated with the CHEK2 p.Ser428Phe Ashkenazi Jewish founder pathogenic variantYael Laitman, Sarah M Nielsen, Kathryn E Hatchell, et al.
Familial Cancer|April 13, 2022
Preimplantation genetic testing in patients with genetic susceptibility to cancerMarie-Charlotte Villy, Nelly Frydman, Céline Moutou, et al.
Familial Cancer|August 19, 2010
An intronic mutation in MLH1 associated with familial colon and breast cancerF Bianchi, M Raponi, F Piva, et al.
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