Jove
Visualize
Contact Us
JoVE
x logofacebook logolinkedin logoyoutube logo
ABOUT JoVE
OverviewLeadershipBlogJoVE Help Center
AUTHORS
Publishing ProcessEditorial BoardScope & PoliciesPeer ReviewFAQSubmit
LIBRARIANS
TestimonialsSubscriptionsAccessResourcesLibrary Advisory BoardFAQ
RESEARCH
JoVE JournalMethods CollectionsJoVE Encyclopedia of ExperimentsArchive
EDUCATION
JoVE CoreJoVE BusinessJoVE Science EducationJoVE Lab ManualFaculty Resource CenterFaculty Site
Terms & Conditions of Use
Privacy Policy
Policies

Filters

Borut Peterlin

Showing results (211-220 of 274) with videos related to

Pageof 28
Sort By:
Clinical Genetics|November 2, 2025
Biallelic RFC1 Expansions Are a Rare Cause of Early-Onset and Familial Parkinson's DiseaseAnja Kovanda, Lara Šušmelj, Helena Jaklič, et al.
Zdravstveno Varstvo|September 21, 2020
Development of an Algorithm for Determining of Genetic Risk at the Primary Healthcare Level - A New Tool for Primary Prevention: A Study ProtocolPolona Selič, Zalika Klemenc-Ketiš, Erika Zelko, et al.
Plos One|December 5, 2023
A novel splice-site FHOD3 founder variant is a common cause of hypertrophic cardiomyopathy in the population of the Balkans-A cohort studyNina Vodnjov, Janez Toplišek, Aleš Maver, et al.
Journal of Neuro-Ophthalmology : the Official Journal of the North American Neuro-Ophthalmology Society|March 10, 2023
Leber Hereditary Optic Neuropathy in a Family of Carriers of MT-ND5 m.13042G>T (A236S) Novel VariantSanja Petrović Pajić, Maja Suštar Habjan, Jelka Brecelj, et al.
Gynecologic and Obstetric Investigation|July 22, 2025
Endometrial Transcriptome Changes following Short-Term Liraglutide Treatment in Infertile Women with Polycystic Ovarian Syndrome and ObesityVesna Salamun, Luca Lovrecic, Ales Maver, et al.
Angiology|March 18, 2004
Sex difference in the effect of ACE-DD genotype on the risk of premature myocardial infarctionDaniel Petrovic, Dejan Bregar, Barbara Guzic-Salobir, 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.
International Journal of Molecular Sciences|July 27, 2024
Genomic Landscape of Susceptibility to Severe COVID-19 in the Slovenian PopulationAnja Kovanda, Tadeja Lukežič, Aleš Maver, et al.
Fertility and Sterility|December 19, 2025
Towards clinical application of whole exome sequencing in the diagnosis of men with severely impaired spermatogenesisRebeka Podgrajsek, Alenka Hodzic, Ales Maver, et al.
Reproductive Biology and Endocrinology : RB&E|November 19, 2025
The role of DNA mismatch repair mutS/mutL homolog genes in spermatogenesis and male infertility: a systematic review and cohort studyRebeka Podgrajsek, Alenka Hodzic, Ales Maver, et al.
Pageof 28

Showing results (211-220 of 274) with videos related to

Sort By:
Pageof 28
Clinical Genetics|November 2, 2025
Biallelic RFC1 Expansions Are a Rare Cause of Early-Onset and Familial Parkinson's DiseaseAnja Kovanda, Lara Šušmelj, Helena Jaklič, et al.
Zdravstveno Varstvo|September 21, 2020
Development of an Algorithm for Determining of Genetic Risk at the Primary Healthcare Level - A New Tool for Primary Prevention: A Study ProtocolPolona Selič, Zalika Klemenc-Ketiš, Erika Zelko, et al.
Plos One|December 5, 2023
A novel splice-site FHOD3 founder variant is a common cause of hypertrophic cardiomyopathy in the population of the Balkans-A cohort studyNina Vodnjov, Janez Toplišek, Aleš Maver, et al.
Journal of Neuro-Ophthalmology : the Official Journal of the North American Neuro-Ophthalmology Society|March 10, 2023
Leber Hereditary Optic Neuropathy in a Family of Carriers of MT-ND5 m.13042G>T (A236S) Novel VariantSanja Petrović Pajić, Maja Suštar Habjan, Jelka Brecelj, et al.
Gynecologic and Obstetric Investigation|July 22, 2025
Endometrial Transcriptome Changes following Short-Term Liraglutide Treatment in Infertile Women with Polycystic Ovarian Syndrome and ObesityVesna Salamun, Luca Lovrecic, Ales Maver, et al.
Angiology|March 18, 2004
Sex difference in the effect of ACE-DD genotype on the risk of premature myocardial infarctionDaniel Petrovic, Dejan Bregar, Barbara Guzic-Salobir, 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.
International Journal of Molecular Sciences|July 27, 2024
Genomic Landscape of Susceptibility to Severe COVID-19 in the Slovenian PopulationAnja Kovanda, Tadeja Lukežič, Aleš Maver, et al.
Fertility and Sterility|December 19, 2025
Towards clinical application of whole exome sequencing in the diagnosis of men with severely impaired spermatogenesisRebeka Podgrajsek, Alenka Hodzic, Ales Maver, et al.
Reproductive Biology and Endocrinology : RB&E|November 19, 2025
The role of DNA mismatch repair mutS/mutL homolog genes in spermatogenesis and male infertility: a systematic review and cohort studyRebeka Podgrajsek, Alenka Hodzic, Ales Maver, et al.
Pageof 28