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High frequency of hereditary colorectal cancer in Newfoundland likely involves novel susceptibility genes.
Woods MO, Hyde AJ, Curtis FK, Stuckless S, Green JS, Pollett AF, Robb JD, Green RC, Croitoru ME, Careen A, Chaulk JA, Jegathesan J, McLaughlin JR, Gallinger SS, Younghusband HB, Bapat BV, Parfrey PS. Woods MO, et al. Among authors: curtis fk. Clin Cancer Res. 2005 Oct 1;11(19 Pt 1):6853-61. doi: 10.1158/1078-0432.CCR-05-0726. Clin Cancer Res. 2005. PMID: 16203774
Cancer prevention in cancer predisposition syndromes: A protocol for testing the feasibility of building a hereditary cancer research registry and nurse navigator follow up model.
Etchegary H, Pike A, Puddester R, Watkins K, Warren M, Francis V, Woods M, Green J, Savas S, Seal M, Gao Z, Avery S, Curtis F, McGrath J, MacDonald D, Burry TN, Dawson L. Etchegary H, et al. PLoS One. 2022 Dec 22;17(12):e0279317. doi: 10.1371/journal.pone.0279317. eCollection 2022. PLoS One. 2022. PMID: 36548287 Free PMC article.
Psychological Distress and Quality of Life in Participants Undergoing Genetic Testing for Arrhythmogenic Right Ventricular Cardiomyopathy Caused by TMEM43 p.S358L: Is It Time to Offer Population-Based Genetic Screening?
Brothers C, Etchegary H, Curtis F, Simmonds C, Houston J, Young TL, Pullman D, Mariathas HH, Connors S, Hodgkinson K. Brothers C, et al. Public Health Genomics. 2021;24(5-6):253-260. doi: 10.1159/000517265. Epub 2021 Sep 9. Public Health Genomics. 2021. PMID: 34500452 Free article.
An intronic mutation in DKC1 in an infant with Høyeraal-Hreidarsson syndrome.
Pearson T, Curtis F, Al-Eyadhy A, Al-Tamemi S, Mazer B, Dror Y, Abish S, Bale S, Compton J, Ray R, Scott P, Der Kaloustian VM. Pearson T, et al. Am J Med Genet A. 2008 Aug 15;146A(16):2159-61. doi: 10.1002/ajmg.a.32412. Am J Med Genet A. 2008. PMID: 18627054 No abstract available.
24 results