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Pavel Tesner

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Journal of Medical Screening|March 27, 2018
Importance of the integrated test in the Down's syndrome screening algorithmDrahomira Springer, Jaroslav Loucky, Pavel Tesner, et al.
European Archives of Oto-Rhino-Laryngology : Official Journal of the European Federation of Oto-Rhino-Laryngological Societies (EUFOS) : Affiliated with the German Society for Oto-Rhino-Laryngology - Head and Neck Surgery|October 6, 2025
Efficacy of first line of bevacizumab in patients with neurofibromatosis 2-related vestibular schwannomasVladimír Koucký, Michaela Jirkovská, Aleš Vlasák, et al.
Cytogenetic and Genome Research|May 9, 2018
Molecular Cytogenetic Diagnostics of Marker Chromosomes: Analysis in Four Prenatal Cases and Long-Term Clinical Evaluation of CarriersPavel Tesner, Marketa Vlckova, Jana Drabova, et al.
Neurology. Genetics|November 3, 2022
Genetic Testing for Malformations of Cortical Development: A Clinical Diagnostic StudyBarbora Straka, Barbora Hermanovska, Lenka Krskova, et al.
Molecular Cytogenetics|May 16, 2018
A boy with developmental delay and mosaic supernumerary inv dup(5)(p15.33p15.1) leading to distal 5p tetrasomy - case report and review of the literaturePavel Tesner, Jana Drabova, Miroslav Stolfa, et al.
Pediatric Neurology|June 14, 2025
Significance of the Absence of Focal Areas of Signal Intensity on Brain Magnetic Resonance Imaging Examinations in Legius SyndromeBorivoj Petrak, Josef Kraus, Sarka Bendova, et al.
European Journal of Paediatric Neurology : EJPN : Official Journal of the European Paediatric Neurology Society|October 9, 2023
Genetic testing in children enrolled in epilepsy surgery program. A real-life studyBarbora Straka, Barbora Splitkova, Marketa Vlckova, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics|September 14, 2024
Clinical and genetic delineation of autosomal recessive and dominant ACTL6B-related developmental brain disordersElisa Cali, Tania Quirin, Clarissa Rocca, et al.
Nucleic Acids Research|November 12, 2023
The Human Phenotype Ontology in 2024: phenotypes around the worldMichael A Gargano, Nicolas Matentzoglu, Ben Coleman, et al.
Pageof 1

Showing results (1-10 of 9) with videos related to

Sort By:
Pageof 1
Journal of Medical Screening|March 27, 2018
Importance of the integrated test in the Down's syndrome screening algorithmDrahomira Springer, Jaroslav Loucky, Pavel Tesner, et al.
European Archives of Oto-Rhino-Laryngology : Official Journal of the European Federation of Oto-Rhino-Laryngological Societies (EUFOS) : Affiliated with the German Society for Oto-Rhino-Laryngology - Head and Neck Surgery|October 6, 2025
Efficacy of first line of bevacizumab in patients with neurofibromatosis 2-related vestibular schwannomasVladimír Koucký, Michaela Jirkovská, Aleš Vlasák, et al.
Cytogenetic and Genome Research|May 9, 2018
Molecular Cytogenetic Diagnostics of Marker Chromosomes: Analysis in Four Prenatal Cases and Long-Term Clinical Evaluation of CarriersPavel Tesner, Marketa Vlckova, Jana Drabova, et al.
Neurology. Genetics|November 3, 2022
Genetic Testing for Malformations of Cortical Development: A Clinical Diagnostic StudyBarbora Straka, Barbora Hermanovska, Lenka Krskova, et al.
Molecular Cytogenetics|May 16, 2018
A boy with developmental delay and mosaic supernumerary inv dup(5)(p15.33p15.1) leading to distal 5p tetrasomy - case report and review of the literaturePavel Tesner, Jana Drabova, Miroslav Stolfa, et al.
Pediatric Neurology|June 14, 2025
Significance of the Absence of Focal Areas of Signal Intensity on Brain Magnetic Resonance Imaging Examinations in Legius SyndromeBorivoj Petrak, Josef Kraus, Sarka Bendova, et al.
European Journal of Paediatric Neurology : EJPN : Official Journal of the European Paediatric Neurology Society|October 9, 2023
Genetic testing in children enrolled in epilepsy surgery program. A real-life studyBarbora Straka, Barbora Splitkova, Marketa Vlckova, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics|September 14, 2024
Clinical and genetic delineation of autosomal recessive and dominant ACTL6B-related developmental brain disordersElisa Cali, Tania Quirin, Clarissa Rocca, et al.
Nucleic Acids Research|November 12, 2023
The Human Phenotype Ontology in 2024: phenotypes around the worldMichael A Gargano, Nicolas Matentzoglu, Ben Coleman, et al.
Pageof 1