еНаука - преглед

Преглед према Аутор Peterlin, B

Приказ резултата 1 до 4 од 4
ГодинаНасловАутор(и)Тип резултатаМп-кат.
2019CLINICAL NEXT GENERATION SEQUENCING REVEALS AN H3F3A GENE AS A NEW POTENTIAL GENE CANDIDATE FOR MICROCEPHALY ASSOCIATED WITH SEVERE DEVELOPMENTAL DELAY, INTELLECTUAL DISABILITY AND GROWTH RETARDATIONMaver, A; Čuturilo, Goran  ; Ruml, Stojanović J; Peterlin, BНаучни чланак
23M23 - Рад у међ. часопису
2019Otopalatodigital syndrome type I: novel characteristics and prenatal manifestations in two siblingsJoksic, I; Čuturilo, Goran  ; Jurisic, A  ; Djuricic, S; Peterlin, B; Mijovic, M; Karadzov, Orlic N; Egic, A; Milovanovic, ZНаучни чланак
23M23 - Рад у међ. часопису
2018The burden of rare genetic variants in genes involved in tumor necrosis factor (TNF) signalling pathway in multiple sclerosis (MS)Peterlin, AM; Maver, Ales; Hodzic, A; Sega, S; Drulovic, Jelena S  ; Novakovic, Ivana V  ; Pekmezovic, Tatjana D  ; Ristic, S; Kapovic, M; Peterlin, BКонференцијски рад
Мп категорија ће бити приказана накнадно.
2000Y-chromosomal diversity in Europe is clinal and influenced primarily by geography, rather than by languageRosser, ZH; Zerjal, T; Hurles, ME; Adojaan, M; Alavantić, Dragan  ; Amorim, A; Amos, W; Armenteros, M; Arroyo, E; Barbujani, G;
Beckman, G; Beckman, L; Bertranpetit, J; Bosch, E; Bradley, DG; Brede, G; Cooper, G; Corte-Real, HBSM; de Knijff, P; Decorte, R; Dubrova, YE; Evgrafov, O; Gilissen, A; Glišić, Sanja (I)  ; Golge, M; Hill, EW; Jeziorowska, A; Kalaydjieva, L; Kayser, M; Kivisild, T; Kravchenko, SA; Krumina, A; Kucinskas, V; Lavinha, J; Livshits, LA; Malaspina, P; Maria, S; McElreavey, K; Meitinger, TA; Mikelsaar, AV; Mitchell, RJ; Nafa, K; Nicholson, J; Norby, S; Pandya, A; Parik, J; Patsalis, PC; Pereira, L; Peterlin, B; Pielberg, G; Prata, ML; Previdere, C; Roewer, L; Rootsi, S; Rubinsztein, DC; Saillard, J; Santos, FR; Stefanescu, G; Sykes, BC; Tolun, A; Villems, R; Tyler-Smith, C; Jobling, MA;
Научни чланак
21aM21a - Рад у међ. часопису изузетних вредности