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Borut Peterlin

Showing results (51-60 of 274) with videos related to

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Molecular Cytogenetics|November 4, 2015
Brachytelephalangic chondrodysplasia punctata caused by new small hemizygous deletion in a boy presenting with hearing lossIrena Vrečar, Gorazd Rudolf, Borut Peterlin, et al.
Frontiers in Cardiovascular Medicine|November 16, 2020
The Role of microRNAs in Heart Failure: A Systematic ReviewAna Peterlin, Karolina Počivavšek, Danijel Petrovič, et al.
Frontiers in Genetics|May 16, 2022
Editorial: The Importance of Genetic Literacy and Education in MedicineNina Pereza, Borut Peterlin, Saša Ostojić, et al.
Metabolic Brain Disease|July 15, 2018
Contemporary scope of inborn errors of metabolism involving epilepsy or seizuresBirutė Tumienė, Borut Peterlin, Aleš Maver, et al.
Reproductive Biomedicine Online|May 13, 2011
Association between male infertility and genetic variability at the PON1/2 and GSTM1/T1 gene lociMarija Volk, Helena Jaklič, Branko Zorn, et al.
BMC Ear, Nose, and Throat Disorders|December 13, 2005
C.35delG/ GJB2 and del(GJB6-D13S1830) mutations in Croatians with prelingual non-syndromic hearing impairmentIgor Medica, Gorazd Rudolf, Manuela Balaban, et al.
Fertility and Sterility|November 16, 2016
Systematic review and meta-analysis of genetic association studies in idiopathic recurrent spontaneous abortionNina Pereza, Saša Ostojić, Miljenko Kapović, et al.
AMIA ... Annual Symposium Proceedings. AMIA Symposium|January 24, 2007
Exploiting semantic relations for literature-based discoveryDimitar Hristovski, Carol Friedman, Thomas C Rindflesch, et al.
Journal of Human Genetics|August 26, 2003
BglII gene polymorphism of the alpha2beta1 integrin gene is a risk factor for diabetic retinopathy in Caucasians with type 2 diabetesMojca Globočnik Petrovič, Marko Hawlina, Borut Peterlin, et al.
Genetic Testing and Molecular Biomarkers|October 26, 2011
Detection of thrombophilic mutations related to spontaneous abortions by a multiplex SNaPshot methodSvetlana Madjunkova, Marija Volk, Borut Peterlin, et al.
Pageof 28

Showing results (51-60 of 274) with videos related to

Sort By:
Pageof 28
Molecular Cytogenetics|November 4, 2015
Brachytelephalangic chondrodysplasia punctata caused by new small hemizygous deletion in a boy presenting with hearing lossIrena Vrečar, Gorazd Rudolf, Borut Peterlin, et al.
Frontiers in Cardiovascular Medicine|November 16, 2020
The Role of microRNAs in Heart Failure: A Systematic ReviewAna Peterlin, Karolina Počivavšek, Danijel Petrovič, et al.
Frontiers in Genetics|May 16, 2022
Editorial: The Importance of Genetic Literacy and Education in MedicineNina Pereza, Borut Peterlin, Saša Ostojić, et al.
Metabolic Brain Disease|July 15, 2018
Contemporary scope of inborn errors of metabolism involving epilepsy or seizuresBirutė Tumienė, Borut Peterlin, Aleš Maver, et al.
Reproductive Biomedicine Online|May 13, 2011
Association between male infertility and genetic variability at the PON1/2 and GSTM1/T1 gene lociMarija Volk, Helena Jaklič, Branko Zorn, et al.
BMC Ear, Nose, and Throat Disorders|December 13, 2005
C.35delG/ GJB2 and del(GJB6-D13S1830) mutations in Croatians with prelingual non-syndromic hearing impairmentIgor Medica, Gorazd Rudolf, Manuela Balaban, et al.
Fertility and Sterility|November 16, 2016
Systematic review and meta-analysis of genetic association studies in idiopathic recurrent spontaneous abortionNina Pereza, Saša Ostojić, Miljenko Kapović, et al.
AMIA ... Annual Symposium Proceedings. AMIA Symposium|January 24, 2007
Exploiting semantic relations for literature-based discoveryDimitar Hristovski, Carol Friedman, Thomas C Rindflesch, et al.
Journal of Human Genetics|August 26, 2003
BglII gene polymorphism of the alpha2beta1 integrin gene is a risk factor for diabetic retinopathy in Caucasians with type 2 diabetesMojca Globočnik Petrovič, Marko Hawlina, Borut Peterlin, et al.
Genetic Testing and Molecular Biomarkers|October 26, 2011
Detection of thrombophilic mutations related to spontaneous abortions by a multiplex SNaPshot methodSvetlana Madjunkova, Marija Volk, Borut Peterlin, et al.
Pageof 28