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Browsing by Author Keckarević-Marković, Milica
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| Issue Date | Title | Author(s) | Type | М-cat. |
|---|---|---|---|---|
| 2013 | 4. Neurophysiologic and clinical characteristic of neuromyotonia in new hereditary neuromuscular disorder | Milic, Rasic V.; Nikodinovic, J.; Mladenovic, J.; De, Jonghe P.; Jordanova, A.; Baets, J.; Zimon, M.; Keckarević Marković, Milica   ; Savic, Pavicevic D.; Todorovic, S. | Article | 21M21 |
| 2019 | A comprehensive mutation study in wide deep-rooted R1 b Serbian pedigree: mutation rates and male relative differentiation capacity of 36 Y-STR markers (✓) | Čokić, Vladan ; Kecmanović, Miljana ; Zgonjanin-Bosić, Dragana; Jakovski, Zlatko; Veljković, Aleksandar ; Katić, Srđan ; Keckarevic-Marković, Milica ; Keckarević, Dusan | Article | 21aM21a |
| 2018 | A familial search – need for haploid markers confirmation | Keckarević Marković, Milica P. ; Mihajlović Milica; Tanasić Vanja; Kecmanović, Miljana M. ; Keckarević, Dušan P. | Conference Paper | Mp. category will be shown later |
| 2008 | A novel 9-bp duplication in the connexin 32 gene causing X-linked Charcot-Marie-Tooth disease | Keckarević-Marković, Milica ; Milić-Rašić, Vedrana M. ; Kecmanović, Miljana ; Keckarević, Dušan P. ; Todorović, Slobodanka; Romac, Stanka | Conference Paper | Mp. category will be shown later |
| 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 | Article | 21M21 |
| 2013 | 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 |
| 2008 | A three generation Serbian family with C263T mutation in MPZ gene | Keckarević-Marković, Milica ; Dačković, J.; Mladenović, J.; Kecmanović, Miljana ; Keckarević, Dušan ; Milić-Rašić, V.; Romac, S. | Conference Paper | Mp. category will be shown later |
| 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 |
| 2005 | Analiza genskih mutacija kod pacijenata sa naslednim neuropatijama | Milić-Rašić, Vedrana; Todorović, Slobodanka; Keckarević-Marković, Milica ; Romac, Stanka | Conference Paper | Mp. category will be shown later |
| 2005 | Analiza genskih mutacija kod pacijenata sa naslednim neuropatijama | Milić Rašić, V.; Todorović, S.; Keckarević-Marković, Milica ; Romac, S. | Book parts | Mp. category will be shown later |
| 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 |
| 2017 | Analysis of mitochondrial dna control region in the domestic dog | V. Tanasić; M. Gagić; Keckarević Marković, Milica P. ; Keckarević, Dušan P. ; Kecmanović, Miljana M. | Conference Paper | Mp. category will be shown later |
| 2023 | Аnalysis of paternal and maternal lineages in Serbian Roma population | Tanasić, V.; Mihajlović, M.; Kecmanović, Miljana ; Keckarević-Marković, Milica ; Keckarević, Dušan | Conference Paper | 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 | 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 |
| 2019 | ARCA3 in Serbian Romani family caused by founder mutation in ANO10 – a genetic approac | Mihajlović, M.; Tanasić, V.; Keckarević, Dušan ; Mladenović, J.; Kecmanović, Miljana ; Keckarević-Marković, Milica | Conference Paper | Mp. category will be shown later |
| 2019 | ARCA3 in Serbian Romani family caused by founder mutation in ANO10 – a genetic approach | Mihajlović Milica; Tanasić Vanja; Keckarević, Dušan P. ; Mladenović Jelena; Kecmanović, Miljana M. ; Keckarević Marković, Milica P. | 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 |
| 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 | Article | 21aM21a |