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Full Name
Keckarević-Marković, Milica
 
Email
milica@bio.bg.ac.rs
 
 
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Publications

Refined By:
Date Issued:  [2000 TO 2009]

Results 1-25 of 33 (Search time: 0.017 seconds).

Issue DateTitleAuthor(s)Rank
120-Jun-2009Congenital cataracts facial dysmorphism neuropathy in Serbian Romani patientsKeckarević-Marković, Milica ; Milić-Rašić, V.; Kecmanović, Miljana ; Keckarević, Dušan ; Romac, S.M34
2Jun-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
3Jun-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
42009&Molekularna analiza Gli3 gena kod pacijenata sa Palister-Halovim sindromomRadivojević, M.; Keckarević-Marković, Milica ; Dačković, J.; Apostolski, S.; Brajušković, Goran ; Romac, S.M64
5Oct-2008Hereditary motor and sensory neuropathy Lom type in a Serbian familyDačković, Jalena; Keckarević-Marković, M. ; Komazec, Z.; Rakočević-Stojanović, V.; Lavrnić, D.; Stević, Z.; Ribarić, K.; Romac, S.; Apostolski, S.
67-Jun-2008A novel 9-bp duplication in the connexin 32 gene causing X-linked Charcot-Marie-Tooth diseaseKeckarević-Marković, Milica ; Milić-Rašić, V.; Kecmanović, Miljana ; Keckarević, D.; Todorović, S.; Romac, S.M34
77-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
831-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
931-May-2008A three generation Serbian family with C263T mutation in MPZ geneKeckarević-Marković, Milica ; Dačković, J.; Mladenović, J.; Kecmanović, Miljana ; Keckarević, Dušan ; Milić-Rašić, V.; Romac, S.M34
1031-May-2008Frequency of the hemochromatosis gene mutations in patients with hereditary hemochromatosis and in control subjects from SerbiaŠarić, M.; Zamurović, L.; Keckarević-Marković, Milica ; Keckarević, Dušan ; Kecmanović, Miljana ; Savić-Pavićević, Dušanka ; Jović, J.; Romac, S.M34
11Mar-2008HD phenocopies - Possible role of saitohin geneJanković, N.; Kecmanović, M. ; Dimitrijević, R.; Keckarević Marković, M. ; Dobričić, V.; Keckarević, D. ; Savić Pavićević, D. ; Romac, S.
1213-Sep-2007Human Y-specific STR haplotypes in population of Serbia and MontenegroStevanović, Miljana ; Dobričić, Valerija; Keckarević, Dušan ; Perović, Aleksandar; Savić Pavićević, Dušanka ; Keckarević Marković, Milica ; Jovanović, Aleksandar; Romac, Stanka
131-Aug-2007Survival of Huntington's disease patients in Serbia: Longer survival in female patientsPekmezovic, Tatjana; Svetel, Marina; Maric, Jelena; Dujmovic-Basuroski, Irena; Dragasevic, Natasa; Keckarevic, Milica ; Romac, Stanka; Kostic, Vladimir S.
1416-Jun-2007Hereditary Motor and Sensory Neuropathy type Lom in Serbian Romani familyKeckarević-Marković, Milica ; Milić-Rašić, V.; Dobričić, V.; Kecmanović, Miljana ; Dimitrijević, R.; Šarić, M.; Savić-Pavićević, Dušanka ; Keckarević, Dušan ; Todorović, S.; Romac, S.M34
1516-Jun-2007Unverricht-Lundborg disease: the first report of genetically confirmed case in SerbiaKecmanović, Miljana ; Ercegovac, M.; Dimitrijević, R.; Dobričić, V.; Keckarević-Marković, Milica ; Savić-Pavićević, Dušanka ; Šarić, M.; Keckarević, Dušan ; Beslać-Bumbaširević, Lj.; Romac, S.M34
162007Frequency of the hemochromatosis gene mutations in patients with hereditary hemochromatosis and in control subjects from Serbia and MontenegroŠarić, M.; Zamurović, Lj.; Keckarević-Marković, Milica ; Keckarević, Dušan ; Kecmanović, Miljana ; Savić-Pavićević, Dušanka ; Jović, J.; Romac, S.M34
17Aug-2006Frequency 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
18Feb-2006Frequency analysis and clinical characterization of different types of spinocerebellar ataxia in Serbian patientsDragašević, Nataša T.; Čuljković, Biljana; Klein, Christine; Ristić, Aleksandar; Keckarević, Milica ; Topisirović, Ivan; Vukosavić, Slobodanka; Svetel, Marina; Kock, Norman; Stefanova, Elka; Romac, Stanka; Kostić, Vladimir S.
195-Sep-2005Friedreich’s ataxia: analysis of mitotic instabilityDobričić, V.; Keckarević-Marković, Milica ; Stevanović, M.; Šarić, M.; Savić, D.; Keckarević, Dušan ; Romac, S.M34
2016-Jul-2005Population 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
21Apr-2005JP-3 gene polymorphism in a healthy population of Serbia and MontenegroKeckarević, M. ; Savić, D. ; Romac, S.
22Feb-2005Yugoslav HD phenocopies analyzed on the presence of mutations in PrP, ferritin and JP-3 genesKeckarević, Milica ; Savić, Dušanka ; Svetel, Marina; Kostić, Vladimir; Vukosavić, Slobodanka; Romac, Stanka
232005Linkage 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
242005Analiza genskih mutacija kod pacijenata sa naslednim neuropatijamaMilić Rašić, V.; Todorović, S.; Keckarević-Marković, Milica ; Romac, S.M45
252005Molekularna genetika distrofinopatijaKeckarević-Marković, Milica ; Romac, S.M45