Istraživači
Milić-Rašić, Vedrana
Results 81-84 of 84
| Issue Date | Title | Author(s) | Type | Мp-cat. |
|---|---|---|---|---|
| 2010 | N88S mutation in the BSCL2 gene in a Serbian family with distal hereditary motor neuropathy type V or Silver syndrome | Rakočević-Stojanović, V.; Milić Rašić, Vedrana  ; Perić, S.  ; Baets, J.; Timmerman, V.; Dierick, I.; Pavlović, S.; De, Jonghe P. | Article | 22M22 |
| 2009 | Mutational analysis of GJB1, MPZ, PMP22, EGR2, and LITAF/SIMPLE in Serbian Charcot-Marie-Tooth patients | Keckarević-Marković, Milica ; Milić-Rašić, Vedrana ; Mladenović, Jelena; Dacković, Jelena; Kecmanović, Miljana ; Keckarević, Dušan ; Savić-Pavićević, Dušanka ; Romac, Stanka | Article | 21M21 |
| 2009 | Congenital cataracts facial dysmorphism neuropathy in Serbian Romani patients | Keckarević-Marković, Milica ; Milić-Rašić, Vedrana M. ; Kecmanović, Miljana ; Keckarević, Dušan P. ; Romac, Stanka | 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 |