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Browsing by Author Keckarević-Marković, Milica


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Showing results 53 to 72 of 100 < previous   next >
Issue DateTitleAuthor(s)Rank
Jun-2019Identification of a broad spectrum of mammalian and avian species using the short fragment of the mitochondrially encoded cytochrome b geneAndrejevic, Marko; Keckarević Marković, Milica ; Bursac, Biljana; Mihajlović, Milica ; Tanasic, Vanja; Kecmanović, Miljana ; Keckarević, Dušan M22
Sep-2022Identifikacija skeletnih ostataka iz 14. veka pronađenih u nekropoli na teritoriji Stare HercegovineMihajlović, Milica ; Tanasić, Vanja; Keckarević-Marković, Milica ; Kecmanović, Miljana ; Keckarević, Dušan M64
2015Is it easy to recognize HINT1 neuropathy (oral presentation)Milić Rašić, V.; Branković, V.; Mladenović, J.; Nikodinović, J.; Kosac, A.; Baets, J.; De Jonghe, P.; Jordanova, A.; Zimon, M.; Keckarević-Marković, Milica ; Savić-Pavićević, Dušanka ; Todorović, S.M34
1-Dec-2001Is the 31 CAG repeat allele of the spinocerebellar ataxia 1 (SCA1) gene locus non-specifically associated with trinucleotide expansion diseases?Savić, Dušanka ; Topisirović, Ivan; Keckarević, Milica ; Keckarević, Dušan ; Major, Tamara; Čuljković, Biljana; Stojković, Oliver; Rakočević-Stojanović, Vidosava; Mladenović, Jelena; Todorović, Slobodanka; Apostolski, Slobodan; Romac, Stanka
Apr-2005JP-3 gene polymorphism in a healthy population of Serbia and MontenegroKeckarević, M. ; Savić, D. ; Romac, S.
15-Feb-2013Lafora disease: Severe phenotype associated with homozygous deletion of the NHLRC1 geneKecmanović, Miljana ; Jović, Nebojša; Čukić, Mirjana; Keckarević Marković, Milica ; Keckarević, Dušan ; Stevanović, Galina; Romac, Stanka
2005Linkage analysis by microsatellite repeats on a Duchenne muscular dystrophy family: a case reportKeckarević-Marković, Milica ; Dobričić, V.; Stevanović, M. ; Šarić, M.; Savić, D.; Keckarević, Dušan ; Romac, S.M34
2022Marker porekla kao adut u forenzičkim analizama DNK u kompleksnim slučajevima iz perspektive Y hromozomaKecmanović, Miljana ; Keckarević-Marković, Milica ; Keckarević, Dušan М45
2014Microsatellite analysis in CMT1A genetic testingGagić, M.; Keckarević-Marković, Milica ; Keckarević, Dušan ; Kecmanović, Miljana ; Mladenović, J.; Milić Rašić, V.; Romac, S.M64
2004' Mogućnosti molekularne dijagnostike hereditarne hemohromatoze tip1 u Srbiji i Crnoj GoriZamurović, Lj.; Šarić, M.; Keckarević-Marković, Milica ; Čuljković, B.; Jović, J.; Romac, S.M64
2009&Molekularna analiza Gli3 gena kod pacijenata sa Palister-Halovim sindromomRadivojević, M.; Keckarević-Marković, Milica ; Dačković, J.; Apostolski, S.; Brajušković, Goran ; Romac, S.M64
2004Molekularna biologija i genotipsko-fenotipske korelacije Fridrajhove ataksijeKeckarević-Marković, Milica ; Branković-Srećković, V.M45
2005Molekularna genetika distrofinopatijaKeckarević-Marković, Milica ; Romac, S.M45
2003Molekularna genetika distrofinopatijaKeckarević-Marković, Milica M45
2003Molekularna genetika migrene razvojnog dobaJančić-Stefanović, J.; Keckarević-Marković, Milica M45
20-Sep-2017Morphological and micromorphological identification of Cannabis pollen and confirmation of marijuana in forensic traces by THCA synthase gene analysisNikolin, B; Gagić, M; Kecmanović, Miljana ; Keckarević, Dušan ; Janaćković, Peđa ; Gavrilović, Milan ; Rajčević, Nemanja ; Keckarević Marković, Milica M64
28-Aug-2017Mutational analysis of 27 Y-chromosomal STRs performed on 85 males from one deep-rooted Serbian pedigreeKecmanović, Miljana ; Čokić, V.; Keckarević-Marković, Milica ; Živković, J.; Jakovski, Z.; Zgonjanin, D.; Keckarević, Dušan M34
Jun-2009Mutational analysis of GJB1, MPZ, PMP22, EGR2, and LITAF/SIMPLE in Serbian Charcot-Marie-Tooth patientsKeckarević Marković, Milica ; Milic-Rasic, Vedrana; Mladenovic, Jelena; Dackovic, Jelena; Kecmanović, Miljana ; Keckarević, Dušan ; Savić Pavićević, Dušanka ; Romac, Stanka
7-Jun-2008Mutations in NHLRC1 gene are predominant cause of Lafora disease in Serbian populationKecmanović, Miljana ; Jović, N.; Keckarević-Marković, Milica ; Dobričić, V.; Keckarević, Dušan ; Ignjatović, P.; Romac, S.M34
25-Jun-2013Mutations in PMP22, MPZ0 and GJB1 in Serbian CMT patients: phenotypes and mechanisms of pathogenicityKeckarević-Marković, Milica ; Kecmanović, Miljana ; Keckarević, Dušan ; Dacković, J.; Mladenović, J.; Milić-Rasić, V.; Romac, S.M34
Showing results 53 to 72 of 100 < previous   next >