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Diagnostics (Basel, Switzerland)|December 23, 2022
Maternal Copy Number Imbalances in Non-Invasive Prenatal Testing: Do They Matter?Michaela Hyblova, Andrej Gnip, Marcel Kucharik, et al.
Folia Microbiologica|January 19, 2024
Analysis of transcriptomics data from COVID-19 patients: a pilot researchDominik Hadzega, Klaudia Babisova, Michaela Hyblova, et al.
Neurogenetics|August 2, 2025
A monoallelic 8q24.3-duplication involving a single protein encoding TSNARE1 gene may be linked to a new leukodystrophyAnton Karabinos, Erika Tomkova, Katarina Tothova, et al.
Bratislavske Lekarske Listy|July 19, 2022
Molecularly confirmed pontocerebellar hypoplasia in a large family from Slovakia with four severely affected childrenEva Radvanska, Zuzana Pos, Andrea Zatkova, et al.
Diagnostics (Basel, Switzerland)|August 14, 2020
Validation of Copy Number Variants Detection from Pregnant Plasma Using Low-Pass Whole-Genome Sequencing in Noninvasive Prenatal Testing-Like SettingsMichaela Hyblova, Maria Harsanyova, Diana Nikulenkov-Grochova, et al.
Journal of Medical Case Reports|March 1, 2022
Dilated cardiomyopathy is a part of the ARV1-associated phenotype: a case reportAnton Karabinos, Michaela Hyblova, Miroslava Eckertova, et al.
Viruses|September 28, 2023
Long COVID Complicated by Fatal Cytomegalovirus and Aspergillus Infection of the Lungs: An Autopsy Case ReportLucia Krivosikova, Tereza Kuracinova, Peter Martanovic, et al.
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