Претрага
Резултати
Genetic testing for monogenic forms of male infertility contributes to the clinical diagnosis of men with idiopathic severe male infertility
[2024]
Podgrajšek, Rebeka; Hodžić, Alenka; Maver, Aleš; Štimpfel, Martin; Anđelić, Aleksander; Miljanović, Olivera; Ristanović, Momčilo 
; Novaković, Ivana V. ; Plaseska-Karanfilska, Dijana; Noveski, Predrag;
Ostojić, Saša; Gršković, Antun; Buretić-Tomljanović, Alena; Peterlin, Borut;
The role of H-Ras gene in tumorigenesis of oral squamous cell carcinoma [2002]
Popović, B. ; Milašin, Jelena ; Jekić, B. ; Novaković, I.
Oncogenic miR-21 and miR-31 clinical relevance in oral cancer: tissue specimens vs. exosomes
[2024]
Lazarevic, Milos ; Trisic, Dijana ; Jaksic-Karisik, Milica ; Jelovac, Drago B ; Nikolic, Nadja S ; Carkic, Jelena ; Milasin, Jelena M
Analysis of the association between MMP-8 gene polymorphisms and the occurrence of adverse effects after acute ischemic stroke treated with recombinant tissue plasminogen activator
[2024]
Dušanović-Pjević, Marija G. ; Grk, Milka B. ; Vojvodić, Ljubica M.; Rašić, Milica ; Perović, Dijana ; Damnjanović, Tatjana M. ; Pešić, Milica ; Jekić, Biljana B.
Analysis of potential association between genetic variants in microRNA genes hsa-miR-499 and hsa-miR-196a2 and prostate cancer risk in Serbian population [2015]
Dobrijević, Zorana Z. ; Savić-Pavićević, Dušanka ; Vučić, Nemanja Lj. ; Cidilko Stefan; Vinka Vukotić; Filipović Nataša; Stanka Romac; Brajušković, Goran
The prevalence of spinal muscular atrophy carriers in pregnant women in Serbia [2025]
Mandic, Ratka; Jankovic, Milena
The coexistence of APC and FH germline variants: a case report of cooccurrence of two hereditary cancer predisposition syndromes in a single patient
[2025]
Bosankić, Brankica; Čuturilo, Goran ; Mijović, Marija; Ruml-Stojanović, Jelena ; Miletić, Aleksandra; Dedović, Maja; Branković, Marija
Analysis of eNOS gene polymorphisms in Serbian patients with rheumatoid arthritis
[2011]
Damnjanović, Tatjana ; Jekić, Biljana ; Bunjevački, Vera ; Novaković, Ivana ; Milić, Vera ; Krajinović, Maja ; Luković, Ljiljana
Partial trisomy of chromosome 10 in a newborn: a case report
[2023]
Komnenić-Radovanović, Milica; Petrović, Bojana ; Maksimović, Nela
A rare case of prenatal Stuve-Wiedemann syndrome presenting with asymmetric femoral involvement [2025]
Joksic, Ivana D; Toljic, Mina; Stankovic, Andjela; Karadzov-Orlic, Natasa TФилтери
По типу
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