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European Journal of Human Genetics : EJHG|October 17, 2024
ERN GENTURIS guidelines on constitutional mismatch repair deficiency diagnosis, genetic counselling, surveillance, quality of life, and clinical managementChrystelle Colas, Léa Guerrini-Rousseau, Manon Suerink, et al.
European Journal of Medical Genetics|November 14, 2021
Endometrial cancer may be part of the MUTYH-associated polyposis cancer spectrumMarie-Charlotte Villy, Julien Masliah-Planchon, Bruno Buecher, et al.
Diseases of the Colon and Rectum|October 10, 2017
Surveillance of Duodenal Polyposis in Familial Adenomatous Polyposis: Should the Spigelman Score Be Modified?Isabelle Sourrouille, Jérémie H Lefèvre, Conor Shields, et al.
Cancer Genetics|June 10, 2015
Somatic c.34G>T KRAS mutation: a new prescreening test for MUTYH-associated polyposis?Adeline Aimé, Florence Coulet, Jeremie H Lefevre, et al.
Annals of Surgical Oncology|January 27, 2009
APC, MYH, and the correlation genotype-phenotype in colorectal polyposisJérémie H Lefevre, Yann Parc, Magali Svrcek, et al.
Familial Cancer|September 19, 2012
Somatic mosaicism and double somatic hits can lead to MSI colorectal tumorsIsabelle Sourrouille, Florence Coulet, Jeremie H Lefevre, et al.
European Journal of Medical Genetics|August 23, 2021
Cancer predisposition and germline CTNNA1 variantsSilvana Lobo, Patrick R Benusiglio, Florence Coulet, et al.
International Journal of Colorectal Disease|March 14, 2018
Metachronous colorectal cancer risk in Lynch syndrome patients-should the endoscopic surveillance be more intensive?Morgan Anyla, Jérémie H Lefevre, Ben Creavin, et al.
Familial Cancer|July 20, 2010
MYH biallelic mutation can inactivate the two genetic pathways of colorectal cancer by APC or MLH1 transversionsJérémie H Lefevre, Chrystelle Colas, Florence Coulet, et al.
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