Keckarević-Marković, Milica
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Full Name
Keckarević-Marković, Milica
Main Affiliation
Email
milica@bio.bg.ac.rs
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Results 1-20 of 20 (Search time: 0.009 seconds).
Issue Date | Title | Author(s) | Rank | |
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1 | Jul-2019 | A comprehensive mutation study in wide deep-rooted R1b Serbian pedigree: mutation rates and male relative differentiation capacity of 36 Y-STR markers | Čokić, Vladan P.; Kecmanović, Miljana ; Zgonjanin Bosić, Dragana; Jakovski, Zlatko; Veljković, Aleksandar; Katić, Srdjan; Keckarević Marković, Milica ; Keckarević, Dušan | M21a |
2 | Jun-2019 | Identification of a broad spectrum of mammalian and avian species using the short fragment of the mitochondrially encoded cytochrome b gene | Andrejevic, Marko; Keckarević Marković, Milica ; Bursac, Biljana; Mihajlović, Milica ; Tanasic, Vanja; Kecmanović, Miljana ; Keckarević, Dušan | M22 |
3 | Mar-2019 | Assessment of mutation rates for PPY23 Y chromosome STR loci in Serbian father-son pairs | Petrovic, Vule; Kecmanović, Miljana ; Keckarević Marković, Milica ; Keckarević, Dušan | M21a |
4 | Nov-2018 | Comparison of different methods of DNA recovery and PCR amplification in STR profiling of casings—a retrospective study | Radojicic, Verica; Keckarević Marković, Milica ; Puac, Feđa; Kecmanović, Miljana ; Keckarević, Dušan | M21 |
5 | Oct-2017 | Differentiation of Cannabis subspecies by THCA synthase gene analysis using RFLP | Cirovic, Natasa; Kecmanović, Miljana ; Keckarević, Dušan ; Keckarević Marković, Milica | |
6 | 2-May-2016 | Genetics of lafora progressive myoclonic epilepsy: Current perspectives | Kecmanović, Miljana ; Keckarević Marković, Milica ; Keckarević, Dušan ; Stevanović, Galina; Jović, Nebojša; Romac, Stanka | |
7 | May-2016 | Analysis of PMP22 duplication and deletion using a panel of six dinucleotide tandem repeats | Gagic, Milica; Keckarević Marković, Milica ; Kecmanović, Miljana ; Keckarević, Dušan ; Mladenovic, Jelena; Dackovic, Jelena; Milic-Rasic, Vedrana; Romac, Stanka | |
8 | Jan-2016 | Clinical and genetic data on Lafora disease patients of Serbian/Montenegrin origin | Kecmanović, Miljana ; Jović, N.; Keckarević Marković, Milica ; Keckarević, Dušan ; Stevanović, G.; Ignjatović, P.; Romac, S. | |
9 | Feb-2014 | A shared haplotype indicates a founder event in unverricht-lundborg disease patients from Serbia | Kecmanović, Miljana ; Ristić, Aleksandar J.; Ercegovac, Marko; Keckarević Marković, Milica ; Keckarević, Dušan ; Sokić, Dragoslav; Romac, Stanka | |
10 | 15-Feb-2013 | Lafora disease: Severe phenotype associated with homozygous deletion of the NHLRC1 gene | Kecmanović, Miljana ; Jović, Nebojša; Čukić, Mirjana; Keckarević Marković, Milica ; Keckarević, Dušan ; Stevanović, Galina; Romac, Stanka | |
11 | Jan-2013 | An algorithm for genetic testing of serbian patients with demyelinating charcot-marie-tooth | Keckarević Marković, Milica P. ; Dackovic, Jelena; Mladenovic, Jelena; Milic-Rasic, Vedrana; Kecmanović, Miljana ; Keckarević, Dušan ; Romac, Stanka | |
12 | Feb-2012 | A novel P66S mutation in exon 3 of the SOD1 gene with early onset and rapid progression | Keckarević, Dušan ; Stević, Zorica; Keckarević Marković, Milica ; Kecmanović, Miljana ; Romac, Stanka | |
13 | Jul-2010 | Schizophrenia and apolipoprotein e gene polymorphism in Serbian population | Kecmanović, Miljana ; Dobričić, Valerija; Dimitrijević, Rajna; Keckarević, Dušan ; Savić Pavićević, Dušanka ; Keckarević Marković, Milica ; Ivkovic, Maja; Romac, Stanka | |
14 | Jul-2010 | Polymorphisms of the prion protein gene (PRNP) in a Serbian population | Dimitrijević, Rajna; Čadež, Ivana; Keckarević Marković, Milica ; Keckarević, Dušan ; Kecmanović, Miljana ; Dobričić, Valerija; Savić Pavićević, Dušanka ; Brajušković, Goran ; Romac, Stanka | |
15 | Jun-2009 | Mutational analysis of GJB1, MPZ, PMP22, EGR2, and LITAF/SIMPLE in Serbian Charcot-Marie-Tooth patients | Keckarević Marković, Milica ; Milic-Rasic, Vedrana; Mladenovic, Jelena; Dackovic, Jelena; Kecmanović, Miljana ; Keckarević, Dušan ; Savić Pavićević, Dušanka ; Romac, Stanka | |
16 | Jun-2009 | Coexistence of Unverricht-Lundborg disease and congenital deafness: Molecular resolution of a complex comorbidity | Kecmanović, Miljana ; Ristić, Aleksandar J.; Sokić, Dragoslav; Keckarević Marković, Milica ; Vojvodić, Nikola; Ercegovac, Marko; Janković, Slavko; Keckarević, Dušan ; Savić Pavićević, Dušanka ; Romac, Stanka | |
17 | Mar-2008 | HD phenocopies - Possible role of saitohin gene | Janković, N.; Kecmanović, M. ; Dimitrijević, R.; Keckarević Marković, M. ; Dobričić, V.; Keckarević, D. ; Savić Pavićević, D. ; Romac, S. | |
18 | 13-Sep-2007 | Human Y-specific STR haplotypes in population of Serbia and Montenegro | Stevanović, Miljana ; Dobričić, Valerija; Keckarević, Dušan ; Perović, Aleksandar; Savić Pavićević, Dušanka ; Keckarević Marković, Milica ; Jovanović, Aleksandar; Romac, Stanka | |
19 | Aug-2006 | Frequency of the hemochromatosis gene mutations in the population of Serbia and Montenegro [2] | Šarić, M.; Zamurović, Lj; Keckarević Marković, M. ; Keckarević, D. ; Stevanović, M. ; Savić Pavićević, D. ; Jović, J.; Romac, Stanka | |
20 | 16-Jul-2005 | Population data on 14 STR loci from population of Serbia and Montenegro (new and renewed data) | Keckarević, Dušan ; Savić, Dušanka ; Keckarević, Milica ; Stevanović, Miljana ; Tarasjev, Aleksej; Čuljković, Biljana; Darmati, Ana; Vukosavić, Slobodanka; Romac, Stanka |