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Browsing by Author Kecmanović, Miljana


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Showing results 1 to 20 of 76  next >
Issue DateTitleAuthor(s)Rank
9-Jul-2012The advancement of molecular diagnostics of CMT in SerbiaKeckarević-Marković, Milica ; Milić-Rašić, V.; Mladenović, J.; Dačković, J.; Kecmanović, Miljana ; Keckarević, Dušan ; Romac, S.M34
Jan-2013An algorithm for genetic testing of serbian patients with demyelinating charcot-marie-toothKeckarević Marković, Milica P. ; Dackovic, Jelena; Mladenovic, Jelena; Milic-Rasic, Vedrana; Kecmanović, Miljana ; Keckarević, Dušan ; Romac, Stanka
2014Analysis of hexanucleotide GGGGCC repeats in the first intron of the C9orf72 geneLabus, O.; Keckarević, Dušan ; Keckarević-Marković, Milica ; Kecmanović, Miljana ; Romac, S.M64
20-Sep-2017Analysis of mitochondrial dna control region in the domestic dogTanasić, V.; Gagić, M.; Keckarević-Marković, Milica ; Keckarević, Dušan ; Kecmanović, Miljana M64
May-2016Analysis of PMP22 duplication and deletion using a panel of six dinucleotide tandem repeatsGagic, Milica; Keckarević Marković, Milica ; Kecmanović, Miljana ; Keckarević, Dušan ; Mladenovic, Jelena; Dackovic, Jelena; Milic-Rasic, Vedrana; Romac, Stanka
20-May-2016Application of rapidly/fast mutated Y- STR loci analzsis in Serbia: haplotype and mutation analysis with nine generation family tree reconstructionKecmanović, Miljana ; Čokić, V.; Keckarević-Marković, Milica ; Keckarević, Dušan M34
2019ARCA3 in Serbian Romani family caused by founder mutation in ANO10 – a genetic approacMihajlović, M.; Tanasić, V.; Keckarević, Dušan ; Mladenović, J.; Kecmanović, Miljana ; Keckarević-Marković, Milica M64
20-Sep-2017Assessment of mutation rates for PPY23 STR loci in Serbian father-son pairsPetrović, V.; Živković, J.; Keckarević-Marković, Milica ; Kecmanović, Miljana ; Keckarević, Dušan M64
Mar-2019Assessment of mutation rates for PPY23 Y chromosome STR loci in Serbian father-son pairsPetrovic, Vule; Kecmanović, Miljana ; Keckarević Marković, Milica ; Keckarević, Dušan M21a
2019Carrier rates of 7 founder mutations associated with single – gene disorders in Serbian Romani population – a pilot studyTanasić, V.; Mihajlović, M.; Keckarević, Dušan ; Mladenović, J.; Kecmanović, Miljana ; Keckarević-Marković, Milica M64
Jan-2016Clinical and genetic data on Lafora disease patients of Serbian/Montenegrin originKecmanović, Miljana ; Jović, N.; Keckarević Marković, Milica ; Keckarević, Dušan ; Stevanović, G.; Ignjatović, P.; Romac, S.
2017Clinical Center for the Lafora Epilepsy Cure Initiative (LECI): Clinical trial readiness for a global curative drug trial (P2.245)Nguyen, V-H.; Duron, RM.; Serratosa, JM.; Minassian, B.; Michelucci, R.; Genton, P.; Sinha, S.; Arabi, M.; Beydoun, A.; Ben-Menachem, E.; Kecmanović, Miljana ; Guilhoto, L.; Whitehouse, W.; Salas-Puig, J.; Martinez- Juarez, I.; Gentry, M.; Bailey, J.; Delgado-Escueta, AV.M34
31-May-2008Coexistence of Unvericht-Lundborg disease and congenital deafness in one Serbian familyKecmanović, Miljana ; Ristić, A.; Sokić, D.; Keckarević-Marković, Milica ; Keckarević, Dušan ; Romac, S.M34
Jun-2009Coexistence of Unverricht-Lundborg disease and congenital deafness: Molecular resolution of a complex comorbidityKecmanović, Miljana ; Ristić, Aleksandar J.; Sokić, Dragoslav; Keckarević Marković, Milica ; Vojvodić, Nikola; Ercegovac, Marko; Janković, Slavko; Keckarević, Dušan ; Savić Pavićević, Dušanka ; Romac, Stanka
9-Sep-2019Comparative analysis of different DNA recovery methods from touch DNA deposited on plastic bags and aluminium foilRadanović, A.; Kecmanović, Miljana ; Tanasić, V.; Mihajlović, M.; Radojičić, V.; Puac, F.; Keckarević-Marković, Milica ; Keckarević, Dušan M34
Nov-2018Comparison of different methods of DNA recovery and PCR amplification in STR profiling of casings—a retrospective studyRadojicic, Verica; Keckarević Marković, Milica ; Puac, Feđa; Kecmanović, Miljana ; Keckarević, Dušan M21
9-Sep-2019Comparison of Globalfiler TM PCR amplification kit and Precision ID Globalfiler TM NGS STR panel – implications on forensic caseworkKeckarević-Marković, Milica ; Tanasić, V.; Mihajlović, M.; Radojičić, V.; Puac, F.; Kecmanović, Miljana ; Keckarević, Dušan M34
Jul-2019A comprehensive mutation study in wide deep-rooted R1b Serbian pedigree: mutation rates and male relative differentiation capacity of 36 Y-STR markersČokić, Vladan P.; Kecmanović, Miljana ; Zgonjanin Bosić, Dragana; Jakovski, Zlatko; Veljković, Aleksandar; Katić, Srdjan; Keckarević Marković, Milica ; Keckarević, Dušan M21a
20-Jun-2009Congenital cataracts facial dysmorphism neuropathy in Serbian Romani patientsKeckarević-Marković, Milica ; Milić-Rašić, V.; Kecmanović, Miljana ; Keckarević, Dušan ; Romac, S.M34
2014Deletion of NHLRC1 gene is founder mutation in Lafora disease patients of Serbian/Montenegrim originKecmanović, Miljana ; Jović, N.; Keckarević-Marković, Milica ; Keckarević, Dušan ; Stevanović, G.; Romac, S.M64
Showing results 1 to 20 of 76  next >