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Alexander Hoischen

Showing results (61-70 of 249) with videos related to

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Inflammatory Bowel Diseases|December 10, 2024
MIP4IBD: An Easy and Rapid Genotyping-by-Sequencing Assay for the Inflammatory Bowel Diseases Risk LociSare Verstockt, Laurens Hannes, Deborah Sarah Jans, et al.
Current Biology : CB|May 19, 2021
Genome of Peştera Muierii skull shows high diversity and low mutational load in pre-glacial EuropeEmma Svensson, Torsten Günther, Alexander Hoischen, et al.
Molecular Genetics and Genomics : MGG|April 11, 2019
Insufficient evidence for a role of SERPINF1 in otosclerosisHanne Valgaeren, Manou Sommen, Matthias Beyens, et al.
The Journal of Molecular Diagnostics : JMD|September 18, 2016
Reliable Next-Generation Sequencing of Formalin-Fixed, Paraffin-Embedded Tissue Using Single Molecule TagsAstrid Eijkelenboom, Eveline J Kamping, Annemiek W Kastner-van Raaij, et al.
Plos One|May 26, 2017
Whole-genome sequencing of spermatocytic tumors provides insights into the mutational processes operating in the male germlineEleni Giannoulatou, Geoffrey J Maher, Zhihao Ding, et al.
American Journal of Human Genetics|July 8, 2021
Next-generation cytogenetics: Comprehensive assessment of 52 hematological malignancy genomes by optical genome mappingKornelia Neveling, Tuomo Mantere, Susan Vermeulen, et al.
Frontiers in Neurology|January 11, 2020
Single Molecule Molecular Inversion Probes for High Throughput Germline Screenings in DystoniaMichaela Pogoda, Franz-Joachim Hilke, Ebba Lohmann, et al.
European Journal of Human Genetics : EJHG|November 7, 2013
A de novo non-sense mutation in ZBTB18 in a patient with features of the 1q43q44 microdeletion syndromeSonja A de Munnik, Sixto García-Miñaúr, Alexander Hoischen, et al.
European Journal of Human Genetics : EJHG|March 27, 2021
Correction: Long-read trio sequencing of individuals with unsolved intellectual disabilityMarc Pauper, Erdi Kucuk, Aaron M Wenger, et al.
European Journal of Human Genetics : EJHG|December 1, 2020
Long-read trio sequencing of individuals with unsolved intellectual disabilityMarc Pauper, Erdi Kucuk, Aaron M Wenger, et al.
Pageof 25

Showing results (61-70 of 249) with videos related to

Sort By:
Pageof 25
Inflammatory Bowel Diseases|December 10, 2024
MIP4IBD: An Easy and Rapid Genotyping-by-Sequencing Assay for the Inflammatory Bowel Diseases Risk LociSare Verstockt, Laurens Hannes, Deborah Sarah Jans, et al.
Current Biology : CB|May 19, 2021
Genome of Peştera Muierii skull shows high diversity and low mutational load in pre-glacial EuropeEmma Svensson, Torsten Günther, Alexander Hoischen, et al.
Molecular Genetics and Genomics : MGG|April 11, 2019
Insufficient evidence for a role of SERPINF1 in otosclerosisHanne Valgaeren, Manou Sommen, Matthias Beyens, et al.
The Journal of Molecular Diagnostics : JMD|September 18, 2016
Reliable Next-Generation Sequencing of Formalin-Fixed, Paraffin-Embedded Tissue Using Single Molecule TagsAstrid Eijkelenboom, Eveline J Kamping, Annemiek W Kastner-van Raaij, et al.
Plos One|May 26, 2017
Whole-genome sequencing of spermatocytic tumors provides insights into the mutational processes operating in the male germlineEleni Giannoulatou, Geoffrey J Maher, Zhihao Ding, et al.
American Journal of Human Genetics|July 8, 2021
Next-generation cytogenetics: Comprehensive assessment of 52 hematological malignancy genomes by optical genome mappingKornelia Neveling, Tuomo Mantere, Susan Vermeulen, et al.
Frontiers in Neurology|January 11, 2020
Single Molecule Molecular Inversion Probes for High Throughput Germline Screenings in DystoniaMichaela Pogoda, Franz-Joachim Hilke, Ebba Lohmann, et al.
European Journal of Human Genetics : EJHG|November 7, 2013
A de novo non-sense mutation in ZBTB18 in a patient with features of the 1q43q44 microdeletion syndromeSonja A de Munnik, Sixto García-Miñaúr, Alexander Hoischen, et al.
European Journal of Human Genetics : EJHG|March 27, 2021
Correction: Long-read trio sequencing of individuals with unsolved intellectual disabilityMarc Pauper, Erdi Kucuk, Aaron M Wenger, et al.
European Journal of Human Genetics : EJHG|December 1, 2020
Long-read trio sequencing of individuals with unsolved intellectual disabilityMarc Pauper, Erdi Kucuk, Aaron M Wenger, et al.
Pageof 25