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Life (Basel, Switzerland)|April 3, 2021
Whole-Genome Sequencing in Diagnostics of Selected Slovenian Undiagnosed Patients with Rare DisordersGaber Bergant, Aleš Maver, Borut Peterlin
Journal of Medical Case Reports|May 20, 2021
Outcomes of vitrectomy for retinal detachment in a patient with Ehlers-Danlos syndrome type IV: a case reportXhevat Lumi, Gaber Bergant, Anila Lumi, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics|September 16, 2017
Comprehensive use of extended exome analysis improves diagnostic yield in rare disease: a retrospective survey in 1,059 casesGaber Bergant, Ales Maver, Luca Lovrecic, et al.
Scientific Reports|November 20, 2025
Creating the Slovenian genome database and browser as a source of comprehensive variation of the Slovenian populationAleš Maver, Peter Juvan, Urška Kotnik, et al.
Neurology. Genetics|May 6, 2022
Biallelic ATOH1 Gene Variant in Siblings With Pontocerebellar Hypoplasia, Developmental Delay, and Hearing LossTanja Višnjar, Aleš Maver, Karin Writzl, et al.
Genes|February 24, 2024
GiOPARK Project: The Genetic Study of Parkinson's Disease in the Croatian PopulationValentino Rački, Gaber Bergant, Eliša Papić, et al.
Movement Disorders : Official Journal of the Movement Disorder Society|January 11, 2020
Loss-of-Function Mutations in NR4A2 Cause Dopa-Responsive Dystonia ParkinsonismThomas Wirth, Louise Laure Mariani, Gaber Bergant, et al.
Journal of Medical Genetics|March 5, 2025
Gene prioritisation for enhancing molecular diagnosis in rare skeletal muscle disease cohortVictoria Lillback, Gaber Bergant, Maria Francesca Di Feo, et al.
NPJ Parkinson'S Disease|November 5, 2022
A multicenter study of genetic testing for Parkinson's disease in the clinical settingAnja Kovanda, Valentino Rački, Gaber Bergant, et al.
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