Researchers
Keckarević, Dušan
Results 61-80 of 113
| Issue Date | Title | Author(s) | Type | Мp-cat. |
|---|---|---|---|---|
| 2017 | Predictive DNA analysis: assesment of Irisplex SNPs for eye color prediction in Serbian population | Mihajlović, M.; Radojičić, V.; Keckarević-Marković, Milica   ; Kecmanović, Miljana ; Keckarević, Dušan | Conference Paper | Mp. category will be shown later |
| 2017 | Assessment of mutation rates for PPY23 STR loci in Serbian father-son pairs | V. Petrović; J. Živković; Keckarević Marković, Milica P. ; Kecmanović, Miljana M. ; Keckarević, Dušan P. | Conference Paper | Mp. category will be shown later |
| 2016 | Genetics of lafora progressive myoclonic epilepsy: Current perspectives | Kecmanović, Miljana ; Keckarević Marković, Milica ; Keckarević, Dušan ; Stevanovic, Galina; Jovic, Nebojsa | Article | Mp. category will be shown later |
| 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; Dačković, Jelena; Milić Rašić, Vedrana ; Romac, Stanka | Article | 21M21 |
| 2016 | Eksperimentalna biohemija : praktikum | Radović, Svetlana ; Lozo, Jelena ; Keckarević, Dušan | Text book | Mp. category will be shown later |
| 2016 | Application of rapidly/fast mutated Y- STR loci analzsis in Serbia: haplotype and mutation analysis with nine generation family tree reconstruction | Kecmanović, Miljana ; Čokić, V.; Keckarević-Marković, Milica ; Keckarević, Dušan | Conference Paper | Mp. category will be shown later |
| 2016 | Application of rapidly/fast mutated Y-STR loci analysis in Serbia: haplotype and mutation analysis with nine generation family tree reconstruction | Kecmanović, Miljana ; Čokić, Vladan ; Keckarević-Marković, Milica ; Keckarević, Dušan | Conference Paper | Mp. category will be shown later |
| 2015 | Clinical and genetic data on Lafora disease patients of Serbian/Montenegrin origin | Kecmanović, Miljana ; Jović, Nebojša ; Keckarević Marković, Milica ; Keckarević, Dušan ; Stevanović, G.; Ignjatović, P.; Romac, S. | Article | 21M21 |
| 2015 | Population analysis of the European standard set (ESS) loci and SE33 locus in a Republic of Serbia | Jakovski Z; Keckarević, Dušan ; Keckarević-Marković, Milica ; Marjanović D | Conference Paper | Mp. category will be shown later |
| 2014 | A shared haplotype indicates a founder event in Unverricht-Lundborg disease patients from Serbia | Kecmanović, Miljana ; Ristić, Aleksandar ; Ercegovac, Marko ; Keckarević-Marković, Milica ; Keckarević, Dušan ; Sokić, Dragoslav ; Romac, Stanka | Article | 23M23 |
| 2014 | Analysis of hexanucleotide GGGGCC repeats in the first intron of the C9orf72 gene | Keckarević, Dušan ; Keckarević-Marković, Milica ; Kecmanović, Miljana ; Stanka Romac | Conference Paper | Mp. category will be shown later |
| 2014 | PALM-LCM in sexual assault cases | Kecmanović, Miljana ; Keckarević, Dušan ; Keckarević-Marković, Milica | Conference Paper | Mp. category will be shown later |
| 2014 | Microsatellite analysis in CMT1A genetic testing | Gagić Milica; Keckarević-Marković, Milica ; Keckarević, Dušan ; Kecmanović, Miljana ; Jelena Mladenović; Milić-Rašić, Vedrana ; Stanka Romac | Conference Paper | Mp. category will be shown later |
| 2014 | Deletion of NHLRC1 gene is founder mutation in Lafora disease patients of Serbian/Montenegrim origin | Kecmanović, Miljana ; Jović, Nebojša ; Keckarević-Marković, Milica ; Keckarević, Dušan ; Stevanović G; Stanka Romac | Conference Paper | Mp. category will be shown later |
| 2014 | Eksperimentalna biohemija : praktikum | Radović, Svetlana ; Lozo, Jelena ; Keckarević, Dušan | Text book | Mp. category will be shown later |
| 2013 | Mutations in PMP22, MPZ0 and GJB1 in Serbian CMT patients: phenotypes and mechanisms of pathogenicity | Keckarević-Marković, Milica ; Kecmanović, Miljana ; Keckarević, Dušan ; Dacković, J.; Mladenović, J.; Milić-Rasić, V.; Romac, S. | Conference Paper | Mp. category will be shown later |
| 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 | Article | 22M22 |
| 2013 | An algorithm for genetic testing of serbian patients with demyelinating charcot-marie-tooth | Keckarević Marković, Milica ; Dačković, Jelena; Mladenovic, Jelena; Milić Rašić, Vedrana ; Kecmanović, Miljana ; Keckarević, Dušan ; Romac, Stanka | Article | 23M23 |
| 2012 | Over-representation of the L144F SOD1 mutation in Serbian ALS patients due to founder effect | Keckarevic, Dusan P ; Stevic, Zorica D; Keckarevic-Markovic, Milica ; Kecmanovic, Miljana ; Romac, Stanka P | Conference Paper | Mp. category will be shown later |
| 2012 | The advancement of molecular diagnostics of CMT in Serbia | Keckarević-Marković, Milica ; Milić-Rašić, V.; Mladenović, J.; Dačković, J.; Kecmanović, Miljana ; Keckarević, Dušan ; Romac, S. | Conference Paper | Mp. category will be shown later |