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Fredrik Persson

Showing results (41-50 of 51) with videos related to

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Diagnostics (Basel, Switzerland)|October 23, 2021
Clinical Validation of Fetal cfDNA Analysis Using Rolling-Circle-Replication and Imaging Technology in Osaka (CRITO Study)Ritsuko Kimata Pooh, Chika Masuda, Risa Matsushika, et al.
Langmuir : the ACS Journal of Surfaces and Colloids|August 9, 2006
Actin filament guidance on a chip: toward high-throughput assays and lab-on-a-chip applicationsMark Sundberg, Richard Bunk, Nuria Albet-Torres, et al.
Genes, Chromosomes & Cancer|April 17, 2012
Clinically significant copy number alterations and complex rearrangements of MYB and NFIB in head and neck adenoid cystic carcinomaMarta Persson, Ywonne Andrén, Christopher A Moskaluk, et al.
European Journal of Human Genetics : EJHG|January 5, 2025
Characterisation of heritable TP53-related cancer syndrome in Sweden-a nationwide study of genotype-phenotype correlations in 90 familiesMeis Omran, Yaxuan Liu, Alexander Sun Zhang, et al.
Current Issues in Molecular Biology|August 27, 2021
Assessment and Clinical Utility of a Non-Next-Generation Sequencing-Based Non-Invasive Prenatal Testing TechnologyUzay Gormus, Alka Chaubey, Suresh Shenoy, et al.
Langmuir : the ACS Journal of Surfaces and Colloids|August 2, 2016
Visualizing the Nonhomogeneous Structure of RAD51 Filaments Using Nanofluidic ChannelsLouise H Fornander, Karolin Frykholm, Joachim Fritzsche, et al.
Cancers|January 21, 2022
Whole-Body MRI Surveillance-Baseline Findings in the Swedish Multicentre Hereditary <i>TP53</i>-Related Cancer Syndrome Study (SWEP53)Meis Omran, Emma Tham, Yvonne Brandberg, et al.
Clinical Cancer Research : an Official Journal of the American Association for Cancer Research|May 19, 2025
Validation of guidelines for genetic investigation of myeloid neoplasms with germline predisposition: results from a prospective cohort studyBianca Tesi, Anna Robelius, Berivan Baskin, et al.
Prenatal Diagnosis|August 21, 2019
Clinical validation of a novel automated cell-free DNA screening assay for trisomies 21, 13, and 18 in maternal plasmaOlle Ericsson, Tarja Ahola, Fredrik Dahl, et al.
Scientific Reports|March 16, 2018
Imaging single DNA molecules for high precision NIPTFredrik Dahl, Olle Ericsson, Olof Karlberg, et al.
Pageof 6

Showing results (41-50 of 51) with videos related to

Sort By:
Pageof 6
Diagnostics (Basel, Switzerland)|October 23, 2021
Clinical Validation of Fetal cfDNA Analysis Using Rolling-Circle-Replication and Imaging Technology in Osaka (CRITO Study)Ritsuko Kimata Pooh, Chika Masuda, Risa Matsushika, et al.
Langmuir : the ACS Journal of Surfaces and Colloids|August 9, 2006
Actin filament guidance on a chip: toward high-throughput assays and lab-on-a-chip applicationsMark Sundberg, Richard Bunk, Nuria Albet-Torres, et al.
Genes, Chromosomes & Cancer|April 17, 2012
Clinically significant copy number alterations and complex rearrangements of MYB and NFIB in head and neck adenoid cystic carcinomaMarta Persson, Ywonne Andrén, Christopher A Moskaluk, et al.
European Journal of Human Genetics : EJHG|January 5, 2025
Characterisation of heritable TP53-related cancer syndrome in Sweden-a nationwide study of genotype-phenotype correlations in 90 familiesMeis Omran, Yaxuan Liu, Alexander Sun Zhang, et al.
Current Issues in Molecular Biology|August 27, 2021
Assessment and Clinical Utility of a Non-Next-Generation Sequencing-Based Non-Invasive Prenatal Testing TechnologyUzay Gormus, Alka Chaubey, Suresh Shenoy, et al.
Langmuir : the ACS Journal of Surfaces and Colloids|August 2, 2016
Visualizing the Nonhomogeneous Structure of RAD51 Filaments Using Nanofluidic ChannelsLouise H Fornander, Karolin Frykholm, Joachim Fritzsche, et al.
Cancers|January 21, 2022
Whole-Body MRI Surveillance-Baseline Findings in the Swedish Multicentre Hereditary <i>TP53</i>-Related Cancer Syndrome Study (SWEP53)Meis Omran, Emma Tham, Yvonne Brandberg, et al.
Clinical Cancer Research : an Official Journal of the American Association for Cancer Research|May 19, 2025
Validation of guidelines for genetic investigation of myeloid neoplasms with germline predisposition: results from a prospective cohort studyBianca Tesi, Anna Robelius, Berivan Baskin, et al.
Prenatal Diagnosis|August 21, 2019
Clinical validation of a novel automated cell-free DNA screening assay for trisomies 21, 13, and 18 in maternal plasmaOlle Ericsson, Tarja Ahola, Fredrik Dahl, et al.
Scientific Reports|March 16, 2018
Imaging single DNA molecules for high precision NIPTFredrik Dahl, Olle Ericsson, Olof Karlberg, et al.
Pageof 6