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Year | Number of Results |
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2020 | 1 |
2022 | 2 |
2023 | 2 |
2024 | 0 |
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Page 1
Genotype-first approach to identify associations between CDH1 germline variants and cancer phenotypes: a multicentre study by the European Reference Network on Genetic Tumour Risk Syndromes.
Lancet Oncol. 2023 Jan;24(1):91-106. doi: 10.1016/S1470-2045(22)00643-X. Epub 2022 Nov 24.
Lancet Oncol. 2023.
PMID: 36436516
Free PMC article.
Lynch syndrome: influence of additional susceptibility variants on cancer risk.
Vibert R, Hasnaoui J, Perrier A, Lefebvre A, Colas C, Dhooge M, Basset N, Chansavang A, Desseignes C, Duval A, Farelly S, Hamzaoui N, Laurent-Puig P, Metras J, Moliere D, Muleris M, Netter J, Touat M, Bielle F, Labreche K, Nicolle R, Perkins G, Warcoin M, Coulet F, Benusiglio PR.
Vibert R, et al. Among authors: desseignes c.
Eur J Hum Genet. 2023 Sep;31(9):1078-1082. doi: 10.1038/s41431-023-01367-z. Epub 2023 Apr 24.
Eur J Hum Genet. 2023.
PMID: 37088804
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[Oncogénétique dans les cancers de l'ovaire].
Desseignés C, Benusiglio P.
Desseignés C, et al.
Rev Prat. 2022 Jun;72(6):639-641.
Rev Prat. 2022.
PMID: 35899665
French.
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[Clinical Cancer Genetics: A guide for the pathologist].
Basset N, Desseignés C, Boucher C, Coulet F, Benusiglio PR.
Basset N, et al. Among authors: desseignes c.
Ann Pathol. 2020 Apr;40(2):63-69. doi: 10.1016/j.annpat.2020.01.003. Epub 2020 Feb 8.
Ann Pathol. 2020.
PMID: 32046877
Review.
French.
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