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Research outputs
Mutations of the K-ras gene in childhood myelodysplastic syndrome
[2000]
Jekić, Biljana Loss of heterozygosity on chromosome 11 in cervical carcinomas
[2000]
Kačar, Katarina; Novaković, Ivana Clinical significance of X chromosome copy number variations
[2023]
Perović, Dijana The association of ACSL1 rs8086 polymorphism with clinicopathological characteristics of colorectal cancer patients
[2023]
Ebtisam, Ajaj; Cvetković, Dragana Clinical variability in two Macedonian families with Arterial tortuosity syndrome
[2018]
Kocova, M.; Kacarska, R.; Kuzevska-Maneva, K.; Prijić, Sergej M. Human leukocyte antigen - B27 and disease susceptibility in Vojvodina, Serbia [2012]
VOJVODIĆ, SVETLANA I.Otopalatodigital Syndrome Type I: Novel Characteristics and Prenatal Manifestations in Two Siblings
[2019]
Joksić, Ivana 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 CHARACTERIZATION OF 16 NOVEL GENETIC VARIANTS IN GENES RELATED TO CHILDHOOD EPILEPSIES [2023]
Anđelković, MarinaEvaluation of the antioxidant potential of Biochaga in vitro [2023]
Živković, LadaFilters
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