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Anja Wagner

Showing results (161-170 of 174) with videos related to

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Journal of Clinical Oncology : Official Journal of the American Society of Clinical Oncology|December 17, 2014
Lynch syndrome caused by germline PMS2 mutations: delineating the cancer riskSanne W ten Broeke, Richard M Brohet, Carli M Tops, 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.
Genetics in Medicine : Official Journal of the American College of Medical Genetics|June 26, 2015
The effect of genotypes and parent of origin on cancer risk and age of cancer development in PMS2 mutation carriersManon Suerink, Heleen M van der Klift, Sanne W Ten Broeke, et al.
Journal of Medical Genetics|January 14, 2018
Role of germline aberrations affecting <i>CTNNA1</i>, <i>MAP3K6</i> and <i>MYD88</i> in gastric cancer susceptibilityRobbert D A Weren, Rachel S van der Post, Ingrid P Vogelaar, et al.
Clinical Cancer Research : an Official Journal of the American Association for Cancer Research|January 21, 2018
High Yield of Pathogenic Germline Mutations Causative or Likely Causative of the Cancer Phenotype in Selected Children with CancerIllja J Diets, Esmé Waanders, Marjolijn J Ligtenberg, et al.
Human Mutation|July 21, 2016
Comprehensive Mutation Analysis of PMS2 in a Large Cohort of Probands Suspected of Lynch Syndrome or Constitutional Mismatch Repair Deficiency SyndromeHeleen M van der Klift, Arjen R Mensenkamp, Mark Drost, et al.
American Journal of Human Genetics|November 20, 2021
Bi-allelic variants in OGDHL cause a neurodevelopmental spectrum disease featuring epilepsy, hearing loss, visual impairment, and ataxiaZheng Yie Yap, Stephanie Efthymiou, Simone Seiffert, et al.
BMJ Open|January 23, 2017
Validation of a clinical screening instrument for tumour predisposition syndromes in patients with childhood cancer (TuPS): protocol for a prospective, observational, multicentre studyFloor A M Postema, Saskia M J Hopman, Corianne A J M de Borgie, et al.
Journal of the National Cancer Institute|December 24, 2009
Risks of Lynch syndrome cancers for MSH6 mutation carriersLaura Baglietto, Noralane M Lindor, James G Dowty, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics|June 18, 2019
An alternative approach to establishing unbiased colorectal cancer risk estimation in Lynch syndromeManon Suerink, Mar Rodríguez-Girondo, Heleen M van der Klift, et al.
Pageof 18

Showing results (161-170 of 174) with videos related to

Sort By:
Pageof 18
Journal of Clinical Oncology : Official Journal of the American Society of Clinical Oncology|December 17, 2014
Lynch syndrome caused by germline PMS2 mutations: delineating the cancer riskSanne W ten Broeke, Richard M Brohet, Carli M Tops, 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.
Genetics in Medicine : Official Journal of the American College of Medical Genetics|June 26, 2015
The effect of genotypes and parent of origin on cancer risk and age of cancer development in PMS2 mutation carriersManon Suerink, Heleen M van der Klift, Sanne W Ten Broeke, et al.
Journal of Medical Genetics|January 14, 2018
Role of germline aberrations affecting <i>CTNNA1</i>, <i>MAP3K6</i> and <i>MYD88</i> in gastric cancer susceptibilityRobbert D A Weren, Rachel S van der Post, Ingrid P Vogelaar, et al.
Clinical Cancer Research : an Official Journal of the American Association for Cancer Research|January 21, 2018
High Yield of Pathogenic Germline Mutations Causative or Likely Causative of the Cancer Phenotype in Selected Children with CancerIllja J Diets, Esmé Waanders, Marjolijn J Ligtenberg, et al.
Human Mutation|July 21, 2016
Comprehensive Mutation Analysis of PMS2 in a Large Cohort of Probands Suspected of Lynch Syndrome or Constitutional Mismatch Repair Deficiency SyndromeHeleen M van der Klift, Arjen R Mensenkamp, Mark Drost, et al.
American Journal of Human Genetics|November 20, 2021
Bi-allelic variants in OGDHL cause a neurodevelopmental spectrum disease featuring epilepsy, hearing loss, visual impairment, and ataxiaZheng Yie Yap, Stephanie Efthymiou, Simone Seiffert, et al.
BMJ Open|January 23, 2017
Validation of a clinical screening instrument for tumour predisposition syndromes in patients with childhood cancer (TuPS): protocol for a prospective, observational, multicentre studyFloor A M Postema, Saskia M J Hopman, Corianne A J M de Borgie, et al.
Journal of the National Cancer Institute|December 24, 2009
Risks of Lynch syndrome cancers for MSH6 mutation carriersLaura Baglietto, Noralane M Lindor, James G Dowty, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics|June 18, 2019
An alternative approach to establishing unbiased colorectal cancer risk estimation in Lynch syndromeManon Suerink, Mar Rodríguez-Girondo, Heleen M van der Klift, et al.
Pageof 18