Претрага

Резултати

Internal Skeletal Dysplasia Registry within the electronic database of Department of Clinical Genetics University Children's Hospital in Belgrade - basis for a personalised medicine in the future [2023]

Mijovic, Marija; Cuturilo, Goran; Ruml-Stojanovic, Jelena; Miletic, Aleksandra; Bosankic, Brankica; Petrovic, Hristina

Chromosomal microarray analysis in children with syndromic short stature [2024]

Maksimović, Nela ; Damnjanović, Tatjana M. ; Jekić, Biljana B. ; Grk, Milka B. ; Dušanović-Pjević, Marija G. ; Đuranović, Ana S. ; Rašić, Milica ; Barzegar, Parsa; El Hayani, Badr; Perović, Dijana

Hereditary angioedema due to C1-inhibitor deficiency in south-eastern Europe: SERPING1 mutations and genetic factors modifying the clinical phenotype [2019]

Rijavec, Matija; Kosnik, Mitja; Zidarn, M; Andrejevic, Sladjana B; Karadza-Lapic, Ljerka; Cikojevic, D; Grivceva-Panovska, Vesna; Korosec, Peter

Increased risk for recurrent pregnancy loss in FXIII V34L and PAI-1 4G/5G compound heterozigots [2019]

Joksic, Ivana D; Joksic, Gordana

Glycogen Storage Disease Type Ib - Case Report [2011]

Kavečan, Ivana ; Jovanović-Privrodski, Jadranka ; Obrenović, Milan; Konstantinidis, Nada; Tomić, Jelena; Jojkić, Pavkov Danijela

Association of genetic markers of coagulation and fibrinolysis with prematurity complication [2019]

Damnjanović, Tatjana M. ; Grk, Milka B. ; Varljen, Tatjana J.; Pantelić, Jelica R.; Maksimović, Nela S. ; Jekić, Biljana B. ; Novaković, Ivana V.

Analysis of association of MMP-2 gene promoter haplotype with efficacy and toxicity of methotrexate in patients with Rheumatoid arthritis [2020]

Grk, Milka B. ; Milić, Vera D. ; Dušanović-Pjević, Marija G. ; Maksimović, Nela S. ; Damnjanović, Tatjana M. ; Pešić, Milica ; Gulić, Milica ; Jekić, Biljana B.

A novel recessive TTN founder variant is a common cause of distal myopathy in the Serbian population. [2017]

Perić, Stojan ; Nikodinović-Glumac, Jelena; Töpf, Ana; Savić-Pavićević, Dušanka ; Phillips, Lauren; Johnson, Katherine; Cassop-Thompson, Marcus; Xu, Liwen; Bertoli, Marta; Lek, Monkol;

MacArthur, Daniel; Brkušanin, Miloš ; Milenković, Sanja ; Milić-Rašić, Vedrana ; Banko, Bojan ; Maksimović, Ružica ; Lochmüller, Hanns; Stojanović, Vidosava ; Straub, Volker;

8 year experience in molecular prenatal diagnostics of cystic fibrosis in Yugoslavia - problems and future trends [1998]

Radojković, Dragica ; Kušić-Tišma, Jelena ; Sretenović, Z; Miletić, S; Niksić, S; Dabović, B; Savić, A

Thalassemia syndromes in Serbia:the importance of genetic (re)analysis [2025]

Ugrin, Milena ; Komazec, Jovana ; Klaassen, Kristel ; Skakic, Anita ; Andjelkovic, Marina ; Spasovski, Vesna ; Stevanovic, Nina ; Parezanovic, Marina ; Stankovic, Sara ; Jocic, Nikola ;

Pavlovic, Sonja; Stojiljkovic, Maja ;