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Borut Peterlin

Showing results (91-100 of 274) with videos related to

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Frontiers in Genetics|August 3, 2023
Case Report: Non-ossifying fibromas with pathologic fractures in a patient with <i>NONO</i>-associated X-linked syndromic intellectual developmental disorderKarin Writzl, Blaž Mavčič, Aleš Maver, et al.
International Journal of Medical Informatics|February 8, 2005
Using literature-based discovery to identify disease candidate genesDimitar Hristovski, Borut Peterlin, Joyce A Mitchell, et al.
The Journal of Maternal-Fetal & Neonatal Medicine : the Official Journal of the European Association of Perinatal Medicine, the Federation of Asia and Oceania Perinatal Societies, the International Society of Perinatal Obstetricians|June 24, 2008
Incidence of the 35delG/GJB2 mutation in low-risk newbornsSanja Zaputovic, Milan Stanojevic, Igor Medica, et al.
Reproductive Biomedicine Online|September 26, 2009
Association between genetic polymorphisms in cytokine genes and recurrent miscarriage--a meta-analysisIgor Medica, Sasa Ostojic, Nina Pereza, et al.
Molecular Genetics & Genomic Medicine|October 24, 2019
Combination of QF-PCR and aCGH is an efficient diagnostic strategy for the detection of chromosome aberrations in recurrent miscarriageLuca Lovrečić, Nina Pereza, Helena Jaklič, et al.
Advances in Medical Sciences|March 1, 2019
Circadian clock genes and circadian phenotypes in patients with myocardial infarctionIvana Škrlec, Jakov Milić, Marija Heffer, et al.
Frontiers in Endocrinology|March 25, 2025
Unraveling the complexity of skeletal dysplasias in the national health systemDorra Najjar, Aleš Maver, Ana Peterlin, et al.
Neurological Sciences : Official Journal of the Italian Neurological Society and of the Italian Society of Clinical Neurophysiology|August 29, 2016
Angiotensin-converting enzyme insertion/deletion gene polymorphism in multiple sclerosis: a meta-analysisSmiljana Ristić, Nada Starčević Čizmarević, Juraj Sepčić, et al.
Journal of Human Genetics|November 18, 2003
A hemochromatosis-causing mutation C282Y is a risk factor for proliferative diabetic retinopathy in Caucasians with type 2 diabetesBorut Peterlin, Mojca Globočnik Petrovič, Jana Makuc, et al.
Cardiology|February 1, 2007
Association of vascular endothelial growth factor gene polymorphism with myocardial infarction in patients with type 2 diabetesDaniel Petrovic, Renata Verhovec, Mojca Globocnik Petrovic, et al.
Pageof 28

Showing results (91-100 of 274) with videos related to

Sort By:
Pageof 28
Frontiers in Genetics|August 3, 2023
Case Report: Non-ossifying fibromas with pathologic fractures in a patient with <i>NONO</i>-associated X-linked syndromic intellectual developmental disorderKarin Writzl, Blaž Mavčič, Aleš Maver, et al.
International Journal of Medical Informatics|February 8, 2005
Using literature-based discovery to identify disease candidate genesDimitar Hristovski, Borut Peterlin, Joyce A Mitchell, et al.
The Journal of Maternal-Fetal & Neonatal Medicine : the Official Journal of the European Association of Perinatal Medicine, the Federation of Asia and Oceania Perinatal Societies, the International Society of Perinatal Obstetricians|June 24, 2008
Incidence of the 35delG/GJB2 mutation in low-risk newbornsSanja Zaputovic, Milan Stanojevic, Igor Medica, et al.
Reproductive Biomedicine Online|September 26, 2009
Association between genetic polymorphisms in cytokine genes and recurrent miscarriage--a meta-analysisIgor Medica, Sasa Ostojic, Nina Pereza, et al.
Molecular Genetics & Genomic Medicine|October 24, 2019
Combination of QF-PCR and aCGH is an efficient diagnostic strategy for the detection of chromosome aberrations in recurrent miscarriageLuca Lovrečić, Nina Pereza, Helena Jaklič, et al.
Advances in Medical Sciences|March 1, 2019
Circadian clock genes and circadian phenotypes in patients with myocardial infarctionIvana Škrlec, Jakov Milić, Marija Heffer, et al.
Frontiers in Endocrinology|March 25, 2025
Unraveling the complexity of skeletal dysplasias in the national health systemDorra Najjar, Aleš Maver, Ana Peterlin, et al.
Neurological Sciences : Official Journal of the Italian Neurological Society and of the Italian Society of Clinical Neurophysiology|August 29, 2016
Angiotensin-converting enzyme insertion/deletion gene polymorphism in multiple sclerosis: a meta-analysisSmiljana Ristić, Nada Starčević Čizmarević, Juraj Sepčić, et al.
Journal of Human Genetics|November 18, 2003
A hemochromatosis-causing mutation C282Y is a risk factor for proliferative diabetic retinopathy in Caucasians with type 2 diabetesBorut Peterlin, Mojca Globočnik Petrovič, Jana Makuc, et al.
Cardiology|February 1, 2007
Association of vascular endothelial growth factor gene polymorphism with myocardial infarction in patients with type 2 diabetesDaniel Petrovic, Renata Verhovec, Mojca Globocnik Petrovic, et al.
Pageof 28