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Tom van Wezel

Showing results (181-190 of 212) with videos related to

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JCO Global Oncology|May 25, 2023
<i>QPOLE</i>: A Quick, Simple, and Cheap Alternative for <i>POLE</i> Sequencing in Endometrial Cancer by Multiplex Genotyping Quantitative Polymerase Chain ReactionAnne Sophie V M Van den Heerik, Natalja T Ter Haar, Lisa Vermij, et al.
Plos One|June 15, 2016
Whole Gene Capture Analysis of 15 CRC Susceptibility Genes in Suspected Lynch Syndrome PatientsAnne M L Jansen, Marije A Geilenkirchen, Tom van Wezel, et al.
Modern Pathology : an Official Journal of the United States and Canadian Academy of Pathology, Inc|June 12, 2023
Discordant Staining Patterns and Microsatellite Results in Tumors of MSH6 Pathogenic Variant CarriersAnne-Sophie van der Werf-'t Lam, Diantha Terlouw, Carli M Tops, et al.
Journal of the National Cancer Institute|March 11, 2021
Prevalence and Prognosis of Lynch Syndrome and Sporadic Mismatch Repair Deficiency in Endometrial CancerCathalijne C B Post, Ellen Stelloo, Vincent T H B M Smit, et al.
British Journal of Cancer|January 24, 2018
Evidence for genetic association between chromosome 1q loci and predisposition to colorectal neoplasiaStephanie A Schubert, Dina Ruano, Fadwa A Elsayed, et al.
British Journal of Cancer|July 26, 2017
Evidence for genetic association between chromosome 1q loci and predisposition to colorectal neoplasiaStephanie A Schubert, Dina Ruano, Fadwa A Elsayed, et al.
European Journal of Human Genetics : EJHG|July 17, 2008
Deciphering the genetics of hereditary non-syndromic colorectal cancerEli Papaemmanuil, Luis Carvajal-Carmona, Gabrielle S Sellick, et al.
Familial Cancer|November 18, 2017
SNP association study in PMS2-associated Lynch syndromeSanne W Ten Broeke, Fadwa A Elsayed, Lisa Pagan, et al.
Gastroenterology|November 18, 2008
Chromosome 8q23.3 and 11q23.1 variants modify colorectal cancer risk in Lynch syndromeJuul T Wijnen, Richard M Brohet, Ronald van Eijk, et al.
Blood Advances|October 3, 2024
Recurrent ETV3::NCOA2 fusions and MAPK pathway mutations in indeterminate dendritic cell histiocytosisPaul G Kemps, F J Sherida H Woei-A-Jin, Koen D Quint, et al.
Pageof 22

Showing results (181-190 of 212) with videos related to

Sort By:
Pageof 22
JCO Global Oncology|May 25, 2023
<i>QPOLE</i>: A Quick, Simple, and Cheap Alternative for <i>POLE</i> Sequencing in Endometrial Cancer by Multiplex Genotyping Quantitative Polymerase Chain ReactionAnne Sophie V M Van den Heerik, Natalja T Ter Haar, Lisa Vermij, et al.
Plos One|June 15, 2016
Whole Gene Capture Analysis of 15 CRC Susceptibility Genes in Suspected Lynch Syndrome PatientsAnne M L Jansen, Marije A Geilenkirchen, Tom van Wezel, et al.
Modern Pathology : an Official Journal of the United States and Canadian Academy of Pathology, Inc|June 12, 2023
Discordant Staining Patterns and Microsatellite Results in Tumors of MSH6 Pathogenic Variant CarriersAnne-Sophie van der Werf-'t Lam, Diantha Terlouw, Carli M Tops, et al.
Journal of the National Cancer Institute|March 11, 2021
Prevalence and Prognosis of Lynch Syndrome and Sporadic Mismatch Repair Deficiency in Endometrial CancerCathalijne C B Post, Ellen Stelloo, Vincent T H B M Smit, et al.
British Journal of Cancer|January 24, 2018
Evidence for genetic association between chromosome 1q loci and predisposition to colorectal neoplasiaStephanie A Schubert, Dina Ruano, Fadwa A Elsayed, et al.
British Journal of Cancer|July 26, 2017
Evidence for genetic association between chromosome 1q loci and predisposition to colorectal neoplasiaStephanie A Schubert, Dina Ruano, Fadwa A Elsayed, et al.
European Journal of Human Genetics : EJHG|July 17, 2008
Deciphering the genetics of hereditary non-syndromic colorectal cancerEli Papaemmanuil, Luis Carvajal-Carmona, Gabrielle S Sellick, et al.
Familial Cancer|November 18, 2017
SNP association study in PMS2-associated Lynch syndromeSanne W Ten Broeke, Fadwa A Elsayed, Lisa Pagan, et al.
Gastroenterology|November 18, 2008
Chromosome 8q23.3 and 11q23.1 variants modify colorectal cancer risk in Lynch syndromeJuul T Wijnen, Richard M Brohet, Ronald van Eijk, et al.
Blood Advances|October 3, 2024
Recurrent ETV3::NCOA2 fusions and MAPK pathway mutations in indeterminate dendritic cell histiocytosisPaul G Kemps, F J Sherida H Woei-A-Jin, Koen D Quint, et al.
Pageof 22