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Publications by authors named "Denis Boidin"

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Characterisation of heterozygous variants in French patients with Lynch syndrome.
Qing Wang, Julie Leclerc, Gaëlle Bougeard, Sylviane Olschwang, Stéphanie Vasseur, Denis Boidin

J Med Genet· July 2020


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MSH2 c.1022T>C, p.Leu341Pro is a founder pathogenic variation and a major cause of Lynch syndrome in the North of France.
Catherine Vermaut, Julie Leclerc, Francis Vasseur, Agnes Wacrenier, Tonio Lovecchio, Denis Boidin

Genes Chromosomes Cancer· February 2020


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Evidence of constitutional MLH1 epimutation associated to transgenerational inheritance of cancer susceptibility.
Michel Crépin, Marie-Claire Dieu, Sophie Lejeune, Fabienne Escande, Denis Boidin

Hum Mutat· January 2012


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