Associated Papers
Characterization of sebaceous and non-sebaceous cutaneous manifestations in patients with lynch syndrome: a systematic review.
Aziz S et al.
Familial Cancer, 2023
36418753 (PubMed )
Supplement: 10689_2022_319_MOESM3_ESM.xlsx › Sup._3_Uninfromative_Cases
Prospective Statewide Study of Universal Screening for Hereditary Colorectal Cancer: The Ohio Colorectal Cancer Prevention Initiative.
Pearlman R et al.
Jco Precision Oncology, 2021
Evaluation of universal immunohistochemical screening of sebaceous neoplasms in a service setting.
Schon K et al.
Clinical and Experimental Dermatology, 2018
Enrichment of mutations in chromatin regulators in people with Rett syndrome lacking mutations in MECP2.
Sajan SA et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics, 2017
27171548 (PubMed )
Supplement: NIHMS769804-supplement-Supplementary___Appendix__online_only_material__etc___2.xls › ExomeVariants
Frequent germline deleterious mutations in DNA repair genes in familial prostate cancer cases are associated with advanced disease.
Leongamornlert D et al.
British Journal of Cancer, 2014
24556621 (PubMed )
Supplement: bjc201430x1.doc
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