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Juul T Wijnen

Showing results (1-10 of 63) with videos related to

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Mutagenesis|February 2, 2012
A review of the genetic background and tumour profiling in familial colorectal cancerTom van Wezel, Anneke Middeldorp, Juul T Wijnen, et al.
Familial Cancer|March 9, 2013
Genetic modifiers of cancer risk in Lynch syndrome: a reviewBente A Talseth-Palmer, Juul T Wijnen, Desma M Grice, et al.
European Journal of Human Genetics : EJHG|December 15, 2011
8q23.3 and 11q23.1 as modifying loci influencing the risk for CRC in Lynch syndromeBente A Talseth-Palmer, Rodney J Scott, Hans F A Vasen, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics|September 12, 2009
Disentangling the Babylonian speech confusion in genetic counseling: an analysis of the reliability and validity of the nomenclature for BRCA1/2 DNA-test results other than pathogenicJoël Vos, Christi J van Asperen, Juul T Wijnen, et al.
Human Mutation|March 31, 2012
Insertion of an SVA element, a nonautonomous retrotransposon, in PMS2 intron 7 as a novel cause of Lynch syndromeHeleen M van der Klift, Carli M Tops, Frederik J Hes, et al.
International Journal of Cancer|March 29, 2013
Reply to Win and JenkinsBente A Talseth-Palmer, Juul T Wijnen, Daniel Barker, et al.
Journal of Medical Genetics|December 13, 2012
Variants of uncertain significance in BRCA1 and BRCA2 assessment of in silico analysis and a proposal for communication in genetic counsellingSetareh Moghadasi, Nandy Hofland, Joyce N Wouts, et al.
Familial Cancer|October 24, 2003
The inframe MSH2 codon 596 deletion is linked with HNPCC and associated with lack of MSH2 protein in tumoursAstrid T Stormorken, Wolfram Müller, Annika Lindblom, et al.
Human Mutation|December 19, 2009
A cell-free assay for the functional analysis of variants of the mismatch repair protein MLH1Mark Drost, Jos e B M Zonneveld, Linda van Dijk, et al.
Molecular Genetics & Genomic Medicine|August 7, 2015
Splicing analysis for exonic and intronic mismatch repair gene variants associated with Lynch syndrome confirms high concordance between minigene assays and patient RNA analysesHeleen M van der Klift, Anne M L Jansen, Niki van der Steenstraten, et al.
Pageof 7

Showing results (1-10 of 63) with videos related to

Sort By:
Pageof 7
Mutagenesis|February 2, 2012
A review of the genetic background and tumour profiling in familial colorectal cancerTom van Wezel, Anneke Middeldorp, Juul T Wijnen, et al.
Familial Cancer|March 9, 2013
Genetic modifiers of cancer risk in Lynch syndrome: a reviewBente A Talseth-Palmer, Juul T Wijnen, Desma M Grice, et al.
European Journal of Human Genetics : EJHG|December 15, 2011
8q23.3 and 11q23.1 as modifying loci influencing the risk for CRC in Lynch syndromeBente A Talseth-Palmer, Rodney J Scott, Hans F A Vasen, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics|September 12, 2009
Disentangling the Babylonian speech confusion in genetic counseling: an analysis of the reliability and validity of the nomenclature for BRCA1/2 DNA-test results other than pathogenicJoël Vos, Christi J van Asperen, Juul T Wijnen, et al.
Human Mutation|March 31, 2012
Insertion of an SVA element, a nonautonomous retrotransposon, in PMS2 intron 7 as a novel cause of Lynch syndromeHeleen M van der Klift, Carli M Tops, Frederik J Hes, et al.
International Journal of Cancer|March 29, 2013
Reply to Win and JenkinsBente A Talseth-Palmer, Juul T Wijnen, Daniel Barker, et al.
Journal of Medical Genetics|December 13, 2012
Variants of uncertain significance in BRCA1 and BRCA2 assessment of in silico analysis and a proposal for communication in genetic counsellingSetareh Moghadasi, Nandy Hofland, Joyce N Wouts, et al.
Familial Cancer|October 24, 2003
The inframe MSH2 codon 596 deletion is linked with HNPCC and associated with lack of MSH2 protein in tumoursAstrid T Stormorken, Wolfram Müller, Annika Lindblom, et al.
Human Mutation|December 19, 2009
A cell-free assay for the functional analysis of variants of the mismatch repair protein MLH1Mark Drost, Jos e B M Zonneveld, Linda van Dijk, et al.
Molecular Genetics & Genomic Medicine|August 7, 2015
Splicing analysis for exonic and intronic mismatch repair gene variants associated with Lynch syndrome confirms high concordance between minigene assays and patient RNA analysesHeleen M van der Klift, Anne M L Jansen, Niki van der Steenstraten, et al.
Pageof 7