Pretraga
Rezultati
Premature centromere separation syndromes: A manifestation of genome instability? [2000]
Potparević, BiljanaX-linked adrenoleukodystrophy: Diagnosis, pathogenesis and prenatal diagnosis
[2006]
Grković, S.; Nikolić, R.; Dordević, M.; Živančević-Simonović, S. Association between inherited thrombophilia in pregnancy and micronucleus frequency in peripheral blood lymphocytes
[2017]
Šošić, Gordana M.; Jović, Nikola Molecular Characterization of Microrna Interference and Aristolochic Acid Intoxication Found in Upper Tract Urothelial Carcinoma in Patients with Balkan Endemic Nephropathy: A Systematic Review of the Current Literature
[2023]
Basic, Dragoslav T Trisomy 21 with a Small Supernumerary Marker Chromosome Derived From Chromosomes 13/21 and 18 [2010]
Niksic, Snezana B; Deretic, VI; Radivojevic-Pilic, Gordana; Ewers, E; Merkas, M; Ziegler, M; Liehr, ThomasPOTENTIAL NEW GENES INVOLVED IN CYSTIC FIBROSIS PHENOTYPE
[2023]
Kusić Tisma, Jelena Ultra-Early Diffuse Lung Disease in an Infant with Pathogenic Variant in Telomerase Reverse Transcriptase (TERT) Gene
[2024]
Višekruna, Jelena; Baša, Mihail; Grba, Tijana; Anđelković, Marina Individual phenotype trait variability as genetic markers of gender susceptibility to spina bifida [2011]
Nikolić, Dejan P.Detection of SIL-TAL1 deletions in T-cell acute lymphoblastic leukemia
[2000]
Bunjevački, Vera The influence of CYP2C8∗3 on carbamazepine serum concentration in epileptic pediatric patients [2016]
Milovanovic, DraganFilteri
Po tipu
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