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Autori: Peterlin Borut

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Naslov Relative preservation of central retinal layers in LHON in comparison to other optic neuropathies (Meeting Abstract)
Autori Petrovic Pajic Sanja MI Lapajne Luka Fakin Ana Jarc-Vidmar Martina Glavac Damjan Volk Marija Maver Ales Vratanar Bor Stare Janez Peterlin Borut Hawlina Marko 
Info INVESTIGATIVE OPHTHALMOLOGY & VISUAL SCIENCE, (2022), vol. 63 br. 7, str. -
Ispravka Web of Science   Elečas   Rang časopisa   Citati: Web of Science  
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Naslov Diagnostic yield of whole exome sequencing in early-onset and familial Parkinson's disease in the Balkans (Meeting Abstract)
Autori Maver Ales Kovanda Anja Bergant Gaber Teran Natasa Vrecar Irena Brankovic Marija  Jankovic Milena Z  Svetel Marina V  Kostic Vladimir S Novakovic Ivana V  Racki Valentino Vuletic Vladimira Peterlin Borut 
Info EUROPEAN JOURNAL OF HUMAN GENETICS, (2022), vol. 30 br. SUPPL 1, Suppl. 1, str. 292-292
Ispravka Web of Science   Elečas   Rang časopisa   Citati: Web of Science  
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Naslov Current State of Compulsory Basic and Clinical Courses in Genetics for Medical Students at Medical Faculties in Balkan Countries With Slavic Languages (Article)
Autori Pereza Nina Terzic Rifet Plaseska-Karanfilska Dijana Miljanovic Olivera Novakovic Ivana V  Poslon Zeljka Ostojic Sasa Peterlin Borut 
Info FRONTIERS IN GENETICS, (2022), vol. 12 br. , str. -
Ispravka Web of Science   Članak   Elečas   Rang časopisa  
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Naslov Maternal LINE-1 DNA Methylation in Early Spontaneous Preterm Birth (Article)
Autori Barisic Anita Stankovic Aleksandra D  Stojkovic Ljiljana  Pereza Nina Ostojic Sasa Peterlin Ana Peterlin Borut Vranekovic Jadranka 
Info BIOLOGICAL RESEARCH FOR NURSING, (2022), vol. 24 br. 1, str. 85-93
Projekat University of Rijeka, Croatia [918.10.0230, 17.07.2.1.04, 18-131]; Slovenian Research Agency - Slovenia [P3-0326]
Ispravka Web of Science   Članak   Elečas   Rang časopisa   Citati: Web of Science   Scopus  
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Naslov De novo mutations in idiopathic male infertility-A pilot study (Article)
Autori Hodzic Alenka Maver Ales Plaseska-Karanfilska Dijana Ristanovic Momcilo Noveski Predrag Zorn Branko Terzic Marija Kunej Tanja Peterlin Borut 
Info ANDROLOGY, (2021), vol. 9 br. 1, str. 212-220
Projekat Slovenian Research Agency - Slovenia [P3-0326]; Ministry of Education and Science of R. Macedonia [17-4523/1]
Ispravka Web of Science   Članak   Elečas   Rang časopisa   Citati: Web of Science   Scopus  
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Naslov Skeletal dysplasia in the era of genomic testing: first experience of a single genetic outpatient clinic from Serbia (Meeting Abstract)
Autori Mijovic Marija Ruml-Stojanovic Jelena Miletic Aleksandra Bosankic Brankica Janeski Hristina Peterlin Borut Maver Ales Cuturilo Goran 
Info EUROPEAN JOURNAL OF HUMAN GENETICS, (2020), vol. 28 br. SUPPL 1, Suppl. 1, str. 831-831
Ispravka Web of Science   Elečas   Rang časopisa   Citati: Web of Science  
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Naslov Phenotype and genotype spectrum of patients with a bilateral optic neuropathy in population of Slovenia (Meeting Abstract)
Autori Petrovic Pajic Sanja MI Jarc-Vidmar Martina Fakin Ana Sustar Maja Brecelj Jelka Lapajne Luka Volk Marija Maver Ales Peterlin Borut Hawlina Marko 
Info INVESTIGATIVE OPHTHALMOLOGY & VISUAL SCIENCE, (2020), vol. 61 br. 7, str. -
Ispravka Web of Science   Elečas   Rang časopisa   Citati: Web of Science  
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Naslov Diagnostic and Clinical Utility of Clinical Exome Sequencing in Children With Moderate and Severe Global Developmental Delay / Intellectual Disability (Article)
Autori Ruml-Stojanovic Jelena Miletic Aleksandra Peterlin Borut Maver Ales Mijovic Marija Borlja Nikola Dimitrijevic Brankica Soldatovic Ivan A  Cuturilo Goran 
Info JOURNAL OF CHILD NEUROLOGY, (2020), vol. 35 br. 2, str. 116-131
Ispravka Web of Science   Članak   Elečas   Rang časopisa   Citati: Web of Science   Scopus  
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Naslov Otopalatodigital Syndrome Type I: Novel Characteristics and Prenatal Manifestations in Two Siblings (Article)
Autori Joksic Ivana D  Cuturilo Goran Jurisic Aleksandar I  Djuricic Slavisa M  Peterlin Borut Mijovic Marija Karadzov-Orlic Natasa T Egic Amira Milovanovic Zagorka M  
Info BALKAN JOURNAL OF MEDICAL GENETICS, (2019), vol. 22 br. 2, str. 83-87
Ispravka Web of Science   Članak   Elečas   Rang časopisa   Citati: Web of Science   Scopus  
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Naslov Clinical Next Generation Sequencing Reveals An H3f3a Gene as a New Potential Gene Candidate for Microcephaly Associated with Severe Developmental Delay, Intellectual Disability and Growth Retardation (Article)
Autori Maver Ales Cuturilo Goran Stojanovic Ruml J Peterlin Borut 
Info BALKAN JOURNAL OF MEDICAL GENETICS, (2019), vol. 22 br. 2, str. 65-68
Projekat Slovenian Research Agency - Slovenia [J3-8205, J3-9280, P3-0326]
Ispravka Web of Science   Članak   Elečas   Rang časopisa   Citati: Web of Science   Scopus  
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