Pretraga
Rezultati
Clinical next generation sequencing reveals an H3F3A gene as a new potential gene candidate for microcephaly associated with severe developmental delay, intellectual disability and growth retardation
[2019]
Maver, Ales; Čuturilo, Goran Hair Depigmentation and Dermatitis - An Unexpected Presentation of Cystic Fibrosis [2013]
Milankov, Olgica; Savic, Radojica N; Tosic, JelaFrequencies of Single-Nucleotide Polymorphisms and Haplotypes of the Slco1b1 Gene in Selected Populations of the Western Balkans [2015]
Grapci, Daka A; Dimovski, AJ; Kapedanovska, A; Vavlukis, Marija; Eftimov, A; Geshkovska, Matevska N; Labachevski, N; Jakjovski, K; Gorani, D; Kedev, Sasko A;
Mladenovska, K;
Frequency of the CFTR 2694T/G polymorphism and its association with CFTR-related monosymptomatic disorders [2001]
Nikolić, AleksandraSox genes and human diseases
[2000]
Stevanović, Milena Cytogenetic and molecular cytogenetic study of Turner's syndrome: a single institution experience [2011]
D. DjordjevicThe Association of ACSL1 and UCP2 3′ Utr Polymorphisms with the Clinicopathological Characteristics of Patients with Colorectal Cancer in Serbia
[2025]
Ajaj, E.; Cvetković, Dragana Townes-Brocks Syndrome With Consistent Renal Hypodysplasia and Variable Extrarenal Features Across Three Generations of Serbian Family
[2025]
Paripović, Aleksandra A Novel 4.2 kb deletion of the 3'UTR of RUNX2 Gene Causes Cleidocranial Dysplasia: Further Delineation of the Role of yhe 3'UTR
[2025]
Mijović, Marija; Čuturilo, Goran Impact of genetics on neoadjuvant therapy with complete pathological response in metastatic colorectal cancer: case report and review of the literature
[2019]
Bulajić, Predrag; Bidžić, Nemanja; Đorđević, Vladimir Filters
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