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miRNA-free rare pathogenic CNVs could drive toward variable CAKUT phenotypes [2022]
Životić, IvanAnalysis of transcripts from alternative PRKAR1B gene promoters in colorectal cancer
[2023]
Pavlović, Dunja Are miR-548 family members potential genetic drivers of CAKUT [2022]
Mitrović, KristinaEP06.016 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, DanijelaComparison of the ABC and ACMG systems for variant classification [2024]
Houge, Gunnar; Bratland, Eirik; Aukrust, Ingvild; Tveten, Kristian; Žukauskaitė, Gabrielė; Sansovic, Ivona; Brea-Fernández, Alejandro J; Mayer, Karin; Paakkola, Teija; McKenna, Caoimhe;
Wright, William; Keckarević-Marković, Milica
; Lildballe, Dorte L; Konecny, Michal; Smol, Thomas; Alhopuro, Pia; Gouttenoire, Estelle Arnaud; Obeid, Katharina; Todorova, Albena; Jankovic, Milena
; Lubieniecka, Joanna M; Stojiljkovic, Maja
; Buisine, Marie-Pierre; Haukanes, Bjørn Ivar; Lorans, Marie; Roomere, Hanno; Petit, François M; Haanpää, Maria K; Beneteau, Claire; Pérez, Belén; Plaseska-Karanfilska, Dijana; Rath, Matthias; Fuhrmann, Nico; Ferreira, Bibiana I; Stephanou, Coralea; Sjursen, Wenche; Maver, Aleš; Rouzier, Cécile; Chirita-Emandi, Adela; Gonçalves, João; Kuek, Wei Cheng David; Broly, Martin; Haer-Wigman, Lonneke; Thong, Meow-Keong; Tae, Sok-Kun; Hyblova, Michaela; den Dunnen, Johan T; Laner, Andreas;
Polymorphisms of ACE and thrombophilic genes: risk for recurrent pregnancy loss
[2024]
Miljanović, Olivera; Ilić, Vesna M.; Likić, Dragan; Teofilov, Slađana; Cikota-Aleksić, Bojana M. Filters
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