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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.AMIA ... Annual Symposium Proceedings. AMIA Symposium|March 31, 2010
Semantic relations for interpreting DNA microarray dataDimitar Hristovski, Andrej Kastrin, Borut Peterlin, et al.Clinical Genetics|July 10, 2024
Streamlined two-step fragment analysis PCR and exome sequencing of RFC1 for diagnostic testing of suspected CANVAS patientsHelena Jaklič, Ivana Babič Božović, Borut Peterlin, et al.Ophthalmologica. Journal International D'Ophtalmologie. International Journal of Ophthalmology. Zeitschrift Fur Augenheilkunde|March 28, 2003
Insertion/deletion plasminogen activator inhibitor 1 and insertion/deletion angiotensin-converting enzyme gene polymorphisms in diabetic retinopathy in type 2 diabetesMojca Globocnik-Petrovic, Marko Hawlina, Borut Peterlin, et al.Journal of Diabetes and Its Complications|March 5, 2005
Aldose reductase (AC)n gene polymorphism and susceptibility to diabetic retinopathy in Type 2 diabetes in CaucasiansMojca Globocnik Petrovic, Borut Peterlin, Marko Hawlina, et al.Prenatal Diagnosis|May 30, 2024
Further exploration of cardiac channelopathy and cardiomyopathy genes in stillbirthMaja Dolanc Merc, Urška Kotnik, Borut Peterlin, et al.Pageof 27