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M Mannens

Showing results (151-160 of 172) with videos related to

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International Journal of Molecular Sciences|July 27, 2022
DNA Methylation Signature for <i>JARID2</i>-Neurodevelopmental SyndromeEline A Verberne, Liselot van der Laan, Sadegheh Haghshenas, et al.
Circulation. Cardiovascular Genetics|December 25, 2009
Desmoglein-2 and desmocollin-2 mutations in dutch arrhythmogenic right ventricular dysplasia/cardiomypathy patients: results from a multicenter studyZahurul A Bhuiyan, Jan D H Jongbloed, Jasper van der Smagt, et al.
Clinical Epigenetics|November 6, 2019
A genome-wide DNA methylation signature for SETD1B-related syndromeI M Krzyzewska, S M Maas, P Henneman, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics|April 30, 2023
DNA methylation episignature and comparative epigenomic profiling of HNRNPU-related neurodevelopmental disorderKathleen Rooney, Liselot van der Laan, Slavica Trajkova, et al.
European Journal of Heart Failure|November 5, 2016
Truncating titin mutations are associated with a mild and treatable form of dilated cardiomyopathyJoeri A Jansweijer, Karin Nieuwhof, Francesco Russo, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics|February 6, 2021
Clinical epigenomics: genome-wide DNA methylation analysis for the diagnosis of Mendelian disordersBekim Sadikovic, Michael A Levy, Jennifer Kerkhof, et al.
The Journal of Clinical Endocrinology and Metabolism|January 18, 2018
Genetic Analyses in Small-for-Gestational-Age NewbornsSusanne E Stalman, Nita Solanky, Miho Ishida, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics|December 21, 2023
DNA methylation episignature, extension of the clinical features, and comparative epigenomic profiling of Hao-Fountain syndrome caused by variants in USP7Liselot van der Laan, Karim Karimi, Kathleen Rooney, et al.
American Journal of Medical Genetics. Part A|March 7, 2022
Genetic care in geographically isolated small island communities: 8 years of experience in the Dutch CaribbeanEline A Verberne, Jonne M Westermann, Tamar I de Vries, et al.
European Heart Journal|April 5, 2011
Manifest disease, risk factors for sudden cardiac death, and cardiac events in a large nationwide cohort of predictively tested hypertrophic cardiomyopathy mutation carriers: determining the best cardiological screening strategyImke Christiaans, Erwin Birnie, Gouke J Bonsel, et al.
Pageof 18

Showing results (151-160 of 172) with videos related to

Sort By:
Pageof 18
International Journal of Molecular Sciences|July 27, 2022
DNA Methylation Signature for <i>JARID2</i>-Neurodevelopmental SyndromeEline A Verberne, Liselot van der Laan, Sadegheh Haghshenas, et al.
Circulation. Cardiovascular Genetics|December 25, 2009
Desmoglein-2 and desmocollin-2 mutations in dutch arrhythmogenic right ventricular dysplasia/cardiomypathy patients: results from a multicenter studyZahurul A Bhuiyan, Jan D H Jongbloed, Jasper van der Smagt, et al.
Clinical Epigenetics|November 6, 2019
A genome-wide DNA methylation signature for SETD1B-related syndromeI M Krzyzewska, S M Maas, P Henneman, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics|April 30, 2023
DNA methylation episignature and comparative epigenomic profiling of HNRNPU-related neurodevelopmental disorderKathleen Rooney, Liselot van der Laan, Slavica Trajkova, et al.
European Journal of Heart Failure|November 5, 2016
Truncating titin mutations are associated with a mild and treatable form of dilated cardiomyopathyJoeri A Jansweijer, Karin Nieuwhof, Francesco Russo, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics|February 6, 2021
Clinical epigenomics: genome-wide DNA methylation analysis for the diagnosis of Mendelian disordersBekim Sadikovic, Michael A Levy, Jennifer Kerkhof, et al.
The Journal of Clinical Endocrinology and Metabolism|January 18, 2018
Genetic Analyses in Small-for-Gestational-Age NewbornsSusanne E Stalman, Nita Solanky, Miho Ishida, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics|December 21, 2023
DNA methylation episignature, extension of the clinical features, and comparative epigenomic profiling of Hao-Fountain syndrome caused by variants in USP7Liselot van der Laan, Karim Karimi, Kathleen Rooney, et al.
American Journal of Medical Genetics. Part A|March 7, 2022
Genetic care in geographically isolated small island communities: 8 years of experience in the Dutch CaribbeanEline A Verberne, Jonne M Westermann, Tamar I de Vries, et al.
European Heart Journal|April 5, 2011
Manifest disease, risk factors for sudden cardiac death, and cardiac events in a large nationwide cohort of predictively tested hypertrophic cardiomyopathy mutation carriers: determining the best cardiological screening strategyImke Christiaans, Erwin Birnie, Gouke J Bonsel, et al.
Pageof 18