Pretraga
Rezultati
Screening for CFTR gene mutations and polymorphisms in patients with chronic pancreatitis [2002]
Nikolić, A
; Kušić-Tišma, Jelena ; Radojković, Dragica ; Lukić, S ; Milosavljević, T ; Savić, A
The importance of comprehensive genomic profiling in differential diagnosis and discovery of novel disease causing genetic variants in patients with pediatric lung diseases
[2019]
Anđelković, Marina ; Minić, Predrag ; Vreća, Miša ; Stojiljković, Maja ; Skakić, Anita ; Sovtić, Aleksandar ; Rodić, M.; Škodrić-Trifunović, Vesna ; Marić, N.; Višekruna, J.;
Spasovski, Vesna ; Pavlović, Sonja ;
; Pavlović, Sonja ; The role of H-Ras gene in tumorigenesis of oral squamous cell carcinoma [2002]
Popović, B. ; Milašin, Jelena ; Jekić, B. ; Novaković, I.
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;
22q11.2 microdeletion is the most common genomic abnormality in Serbian newborns with critical congenital heart disease and could be rapidly detected by Multiplex ligation probe amplification analysis
[2023]
Miletić, Aleksandra; Cuturilo, Goran; Ruml Stojanović, Jelena; Drakulić, Danijela ; Mijović, Marija; Bosankić, Brankica; Petrović, Hristina; Stevanović, Milena
Cytogenetic and molecular genetic characterization of patients with neuroblastoma in Yugoslavia [2002]
Djurisic, Marina; Guc-Scekic, Marija P; Radivojevic, Danijela; Lalic, Tanja; Djuricic, Slavisa M; Djokic, DraganWhole mitochondrial genome analysis in carriers of mt3460 mutation with Leber's hereditary optic neuropathy
[2019]
Dawod, Phepy G. A.; Rovčanin, Branislav R. ; Branković, Marija ; Marjanović, Ana ; Janković, Milena Z. ; Novaković, Ivana V. ; Motaleb, Abdel F.; Jančić, Jasna B. ; Kostić, Vladimir S.
The role of A2ML1 variants in Noonan syndrome remains unverified [2020]
Brinkmann, Julia; ...; Cuturilo, Goran; ...; (broj, koautora 24)Genotype-phenotype correlations in a group of Yugoslavian adult cystic fibrosis patients [2002]
Radivojevic, Danijela; Djurisic, Marina; Minic, Predrag B; Guc-Scekic, Marija P; Lalic, TanjaFilters
By type
- 176