Stefan Aretz
0000-0002-5228-1890
7 papers found
Refreshing results…
Variant profiling of colorectal adenomas from three patients of two families with MSH3-related adenomatous polyposis
No Difference in Penetrance between Truncating and Missense/Aberrant Splicing Pathogenic Variants in MLH1 and MSH2: A Prospective Lynch Syndrome Database Study
The Management of Peutz–Jeghers Syndrome: European Hereditary Tumour Group (EHTG) Guideline
Hereditary Diffuse Gastric Cancer: A Comparative Cohort Study According to Pathogenic Variant Status
Risk-Reducing Gynecological Surgery in Lynch Syndrome: Results of an International Survey from the Prospective Lynch Syndrome Database
Associations of Pathogenic Variants in MLH1, MSH2, and MSH6 With Risk of Colorectal Adenomas and Tumors and With Somatic Mutations in Patients With Lynch Syndrome
Prevalence of CNV-neutral structural genomic rearrangements in MLH1, MSH2, and PMS2 not detectable in routine NGS diagnostics
Missing publications? Search for publications with a matching author name.