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Borut Peterlin

Showing results (121-130 of 274) with videos related to

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Plos One|May 17, 2018
Genetic variation in the CLOCK gene is associated with idiopathic recurrent spontaneous abortionAlenka Hodžić, Polona Lavtar, Momčilo Ristanović, et al.
Acta Clinica Croatica|June 7, 2019
ASSOCIATION OF CIRCADIAN RHYTHM WITH MYOCARDIAL INFARCTIONIvana Škrlec, Jakov Milić, Marija Heffer, 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 2, 2011
The insulin-like growth factor 2 receptor gene Gly1619Arg polymorphism and idiopathic recurrent spontaneous abortionNina Pereza, Saša Ostojić, Marija Volk, et al.
Plos One|January 3, 2018
Diagnostic outcomes of exome sequencing in patients with syndromic or non-syndromic hearing lossTina Likar, Mensuda Hasanhodžić, Nataša Teran, et al.
Fertility and Sterility|March 12, 2013
Genetic variation in tissue inhibitors of metalloproteinases as a risk factor for idiopathic recurrent spontaneous abortionNina Pereza, Marija Volk, Nikolina Zrakić, et al.
Movement Disorders Clinical Practice|January 12, 2026
Two Cases of SPEN Haploinsufficiency Presenting with Dystonia: Expanding the Genotype and PhenotypeLisa Buikema, Matej Lokar, Saman Vinke, 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.
Collegium Antropologicum|January 20, 2009
De novo NEMO gene deletion (delta4-10)--a cause of incontinentia pigmenti in a female infant: a case reportVida Culić, Dragana Gabrić, Neira Puizina-Ivić, et al.
Biomedical Reports|October 20, 2021
Potential protective role of a NOD2 polymorphism in the susceptibility to multiple sclerosis is not associated with interferon therapyAida Zečkanović, Aleš Maver, Smiljana Ristić, 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|August 27, 2019
Genetic variation in the maternal vitamin D receptor FokI gene as a risk factor for recurrent pregnancy lossAnita Barišić, Nina Pereza, Alenka Hodžić, et al.
Pageof 28

Showing results (121-130 of 274) with videos related to

Sort By:
Pageof 28
Plos One|May 17, 2018
Genetic variation in the CLOCK gene is associated with idiopathic recurrent spontaneous abortionAlenka Hodžić, Polona Lavtar, Momčilo Ristanović, et al.
Acta Clinica Croatica|June 7, 2019
ASSOCIATION OF CIRCADIAN RHYTHM WITH MYOCARDIAL INFARCTIONIvana Škrlec, Jakov Milić, Marija Heffer, 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 2, 2011
The insulin-like growth factor 2 receptor gene Gly1619Arg polymorphism and idiopathic recurrent spontaneous abortionNina Pereza, Saša Ostojić, Marija Volk, et al.
Plos One|January 3, 2018
Diagnostic outcomes of exome sequencing in patients with syndromic or non-syndromic hearing lossTina Likar, Mensuda Hasanhodžić, Nataša Teran, et al.
Fertility and Sterility|March 12, 2013
Genetic variation in tissue inhibitors of metalloproteinases as a risk factor for idiopathic recurrent spontaneous abortionNina Pereza, Marija Volk, Nikolina Zrakić, et al.
Movement Disorders Clinical Practice|January 12, 2026
Two Cases of SPEN Haploinsufficiency Presenting with Dystonia: Expanding the Genotype and PhenotypeLisa Buikema, Matej Lokar, Saman Vinke, 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.
Collegium Antropologicum|January 20, 2009
De novo NEMO gene deletion (delta4-10)--a cause of incontinentia pigmenti in a female infant: a case reportVida Culić, Dragana Gabrić, Neira Puizina-Ivić, et al.
Biomedical Reports|October 20, 2021
Potential protective role of a NOD2 polymorphism in the susceptibility to multiple sclerosis is not associated with interferon therapyAida Zečkanović, Aleš Maver, Smiljana Ristić, 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|August 27, 2019
Genetic variation in the maternal vitamin D receptor FokI gene as a risk factor for recurrent pregnancy lossAnita Barišić, Nina Pereza, Alenka Hodžić, et al.
Pageof 28