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Research outputs
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, A; Čuturilo, Goran![](/image/people_icon_ico.png)
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Otopalatodigital syndrome type I: novel characteristics and prenatal manifestations in two siblings [2019]
Joksic, I; Čuturilo, Goran![](/image/people_icon_ico.png)
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Human leukocyte antigen - B27 and disease susceptibility in Vojvodina, Serbia [2012]
VOJVODIĆ, SVETLANA I.![](/image/people_icon_ico.png)
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Evaluation of the antioxidant potential of Biochaga in vitro [2023]
Živković, Lada![](/image/people_icon_ico.png)
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Stem Cells for Periodontal Regeneration (✓) [2013]
Pejčić, Ana![](/image/people_icon_ico.png)
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Individual phenotype trait variability as genetic markers of gender susceptibility to spina bifida [2011]
Nikolić, Dejan P.![](/image/people_icon_ico.png)
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Association between inherited thrombophilia in pregnancy and micronucleus frequency in peripheral blood lymphocytes [2017]
Šošić, Gordana M.; Jović, Nikola; Rakić, Boban; Dimitrijević, Aleksandra![](/image/people_icon_ico.png)
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Detection of SIL-TAL1 deletions in T-cell acute lymphoblastic leukemia (✓) [2000]
Bunjevački, Vera![](/image/people_icon_ico.png)
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Ugt1a1 (ta)(n) promoter genotype: diagnostic and population pharmacogenetic marker in Serbia (✓) [2018]
Vuković, Marija; Radlović, Nedeljko; Leković, Zoran![](/image/people_icon_ico.png)
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Intellectual ability in the Duchenne muscular dystrophy and dystrophin gene mutation location [2014]
Milić Rašić, Vedrana![](/image/people_icon_ico.png)
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