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Challenges in periodic revision of genetic testing results: Comparison of the main classification guidelines and report of a retrospective analysis involving BRCA1/BRCA2 variants of uncertain significance.
Andreis TF, de Souza KIW, Vieira IA, Alemar B, Sinigaglia M, de Araújo Rocha YM, Artigalás O, Bittar C, Oliveira Netto CB, Ashton-Prolla P, Rosset C. Andreis TF, et al. Among authors: rosset c. Gene. 2023 Apr 30;862:147281. doi: 10.1016/j.gene.2023.147281. Epub 2023 Feb 10. Gene. 2023. PMID: 36775216
Vitamin D Status and VDR Genotype in NF1 Patients: A Case-Control Study from Southern Brazil.
Souza Mario Bueno L, Rosset C, Aguiar E, Pereira Fde S, Izetti Ribeiro P, Scalco R, Matzenbacher Bittar C, Brinckmann Oliveira Netto C, Gischkow Rucatti G, Chies JA, Camey SA, Ashton-Prolla P. Souza Mario Bueno L, et al. Among authors: rosset c. Int J Endocrinol. 2015;2015:402838. doi: 10.1155/2015/402838. Epub 2015 Jun 16. Int J Endocrinol. 2015. PMID: 26161090 Free PMC article.
Germline MLH1, MSH2 and MSH6 variants in Brazilian patients with colorectal cancer and clinical features suggestive of Lynch Syndrome.
Schneider NB, Pastor T, Paula AE, Achatz MI, Santos ÂRD, Vianna FSL, Rosset C, Pinheiro M, Ashton-Prolla P, Moreira MÂM, Palmero EI; Brazilian Lynch Syndrome Study Group. Schneider NB, et al. Among authors: rosset c. Cancer Med. 2018 May;7(5):2078-2088. doi: 10.1002/cam4.1316. Epub 2018 Mar 25. Cancer Med. 2018. PMID: 29575718 Free PMC article.
37 results