Researchers
Keckarević-Marković, Milica
Results 101-120 of 132
| Issue Date | Title | Author(s) | Type | Мp-cat. |
|---|---|---|---|---|
| 2008 | Coexistence of Unvericht-Lundborg disease and congenital deafness in one Serbian family | Kecmanović, Miljana | Conference Paper | Mp. category will be shown later |
| 2008 | HD phenocopies - Possible role of saitohin gene![]() | Janković, N.; Kemanović, M. | Article | 23M23 |
| 2008 | Hereditary motor and sensory neuropathy Lom type in a Serbian family | Dačković, Jalena; Keckarević-Marković, M. | Article | 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 | Conference Paper | Mp. category will be shown later |
| 2007 | Human Y-specific STR haplotypes in population of Serbia and Montenegro | Stevanović, Miljana | Article | 21M21 |
| 2007 | Hereditary motor and sensory neuropathy type Lom in Serbian Romany family | Keckarević-Marković, Milica | Conference Paper | Mp. category will be shown later |
| 2007 | Unverricht-Lundborg disease - the first report of genetically confirmed case in Serbia | Kecmanović, Miljana M. | Conference Paper | Mp. category will be shown later |
| 2007 | Survival of Huntington's disease patients in Serbia: Longer survival in female patients | Pekmezovic, Tatjana | Article | 22M22 |
| 2007 | Hereditary Motor and Sensory Neuropathy type Lom in Serbian Romani family | Keckarević-Marković, Milica | Conference Paper | Mp. category will be shown later |
| 2007 | Frequency of the hemochromatosis gene mutations in patients with hereditary hemochromatosis and in control subjects from serbia and montenegro | Šarić, M.; Zamurović, Lj.; Kečkarević-Marković, M. | Conference Paper | Mp. category will be shown later |
| 2006 | Frequency of the hemochromatosis gene mutations in the population of Serbia and Montenegro![]() | Šarić, M.; Zamurović, Ljubica; Keckarević-Marković, Milica | Other | Mp. category will be shown later |
| 2006 | Frequency analysis and clinical characterization of different types of spinocerebellar ataxia in Serbian patients | Dragašević-Mišković, Nataša | Article | 21M21 |
| 2005 | Analiza genskih mutacija kod pacijenata sa naslednim neuropatijama | Milić-Rašić, Vedrana; Todorović, Slobodanka; Keckarević-Marković, Milica | Conference Paper | Mp. category will be shown later |
| 2005 | Molekularna genetika distrofinopatija | Keckarević-Marković, Milica | Book parts | Mp. category will be shown later |
| 2005 | Clinical characteristics and natural history of patients with spinocerebellar ataxia in Serbia | Dragašević-Mišković, Nataša | Conference Paper | Mp. category will be shown later |
| 2005 | Parentalna dijagnostika | Romac, Stanka; Savić-Pavićević, Dušanka | Article | Mp. category will be shown later |
| 2005 | Molekularna genetika distrofinopatija | Keckarević-Marković, Milica | 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 | Book parts | Mp. category will be shown later |
| 2005 | Yugoslav HD phenocopies analyzed on the presence of mutations in PrP, ferritin, and JP-3 genes | Keckarević-Marković, Milica | Article | 23M23 |
| 2005 | JP-3 gene polymorphism in a healthy population of Serbia and Montenegro | Keckarević, M. | Article | 23M23 |
