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Oliver Stojkovic

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Blood Coagulation & Fibrinolysis : an International Journal in Haemostasis and Thrombosis|February 8, 2021
Combinations of fibrinolytic gene polymorphisms (plasminogen activator inhibitor type 1 4G/5G, factor XIII Val34Leu and angiotensin-converting enzyme I/D) in women with idiopathic infertilityJelena Velickovic, Mihajlo Jelicic, Oliver Stojkovic
Human Fertility (Cambridge, England)|September 18, 2018
Polymorphisms and haplotypes in VDR gene are associated with female idiopathic infertilityJelena Djurovic, Gorana Stamenkovic, Jelena Todorovic, et al.
Blood Coagulation & Fibrinolysis : an International Journal in Haemostasis and Thrombosis|July 2, 2019
Hemostasis-related gene polymorphisms and their epistatic relationship in women with idiopathic infertilityJelena Velickovic, Katarina Zeljic, Jelena Todorovic, et al.
Forensic Science International. Genetics|October 19, 2011
Y-chromosomal microsatellite diversity in three culturally defined regions of historical TibetTenzin Gayden, Areej Bukhari, Shilpa Chennakrishnaiah, et al.
The Journal of Sports Medicine and Physical Fitness|December 14, 2023
Principal components analysis to evaluate complex association of polymorphisms in ACE and ACTN3 genes and the extent of cardiovascular adaptive changes in elite athletesTijana Petrovic, Marina Djelic, Marija Zdravkovic, et al.
Journal of Neurogenetics|December 12, 2003
Prevalence of the fragile X syndrome in Yugoslav patients with non-specific mental retardationTamara Major, Biljana Culjkovic, Oliver Stojkovic, et al.
Human Fertility (Cambridge, England)|November 19, 2016
Genetics of suspected thrombophilia in Serbian females with infertility, including three cases, homozygous for FII 20210A or FV 1691A mutationsJelena Djurovic, Oliver Stojkovic, Jelena Todorovic, et al.
Journal of Pediatric Hematology/Oncology|May 1, 2012
Monitoring of pediatric patients with malignant hematological diseases after allogeneic HSCT: Serbian experienceAleksandra Drago Krstic, Oliver Stojkovic, Marija Guc-Scekic, et al.
Legal Medicine (Tokyo, Japan)|January 18, 2011
Y-STR profiling in two Afghanistan populationsHarlette Lacau, Areej Bukhari, Tenzin Gayden, et al.
Gene|September 4, 2016
Corrigendum to "On the Bantu expansion" [GENE 593/1 (2016) 48-57]Daine J Rowold, David Perez-Benedico, Oliver Stojkovic, et al.
Pageof 2

Showing results (1-10 of 17) with videos related to

Sort By:
Pageof 2
Blood Coagulation & Fibrinolysis : an International Journal in Haemostasis and Thrombosis|February 8, 2021
Combinations of fibrinolytic gene polymorphisms (plasminogen activator inhibitor type 1 4G/5G, factor XIII Val34Leu and angiotensin-converting enzyme I/D) in women with idiopathic infertilityJelena Velickovic, Mihajlo Jelicic, Oliver Stojkovic
Human Fertility (Cambridge, England)|September 18, 2018
Polymorphisms and haplotypes in VDR gene are associated with female idiopathic infertilityJelena Djurovic, Gorana Stamenkovic, Jelena Todorovic, et al.
Blood Coagulation & Fibrinolysis : an International Journal in Haemostasis and Thrombosis|July 2, 2019
Hemostasis-related gene polymorphisms and their epistatic relationship in women with idiopathic infertilityJelena Velickovic, Katarina Zeljic, Jelena Todorovic, et al.
Forensic Science International. Genetics|October 19, 2011
Y-chromosomal microsatellite diversity in three culturally defined regions of historical TibetTenzin Gayden, Areej Bukhari, Shilpa Chennakrishnaiah, et al.
The Journal of Sports Medicine and Physical Fitness|December 14, 2023
Principal components analysis to evaluate complex association of polymorphisms in ACE and ACTN3 genes and the extent of cardiovascular adaptive changes in elite athletesTijana Petrovic, Marina Djelic, Marija Zdravkovic, et al.
Journal of Neurogenetics|December 12, 2003
Prevalence of the fragile X syndrome in Yugoslav patients with non-specific mental retardationTamara Major, Biljana Culjkovic, Oliver Stojkovic, et al.
Human Fertility (Cambridge, England)|November 19, 2016
Genetics of suspected thrombophilia in Serbian females with infertility, including three cases, homozygous for FII 20210A or FV 1691A mutationsJelena Djurovic, Oliver Stojkovic, Jelena Todorovic, et al.
Journal of Pediatric Hematology/Oncology|May 1, 2012
Monitoring of pediatric patients with malignant hematological diseases after allogeneic HSCT: Serbian experienceAleksandra Drago Krstic, Oliver Stojkovic, Marija Guc-Scekic, et al.
Legal Medicine (Tokyo, Japan)|January 18, 2011
Y-STR profiling in two Afghanistan populationsHarlette Lacau, Areej Bukhari, Tenzin Gayden, et al.
Gene|September 4, 2016
Corrigendum to "On the Bantu expansion" [GENE 593/1 (2016) 48-57]Daine J Rowold, David Perez-Benedico, Oliver Stojkovic, et al.
Pageof 2