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The Expanding Phenotypical Spectrum of WARS2-Related Disorder: Four Novel Cases with a Common Recurrent Variant.
Genes (Basel). 2023 Mar 29;14(4):822. doi: 10.3390/genes14040822.
Genes (Basel). 2023.
PMID: 37107582
Free PMC article.
Review.
DNMT3B rs2424913 as a Risk Factor for Congenital Heart Defects in Down Syndrome.
Majstorović D, Barišić A, Božović IB, Čače IB, Čače N, Štifanić M, Vraneković J.
Majstorović D, et al. Among authors: bozovic ib.
Genes (Basel). 2023 Feb 24;14(3):576. doi: 10.3390/genes14030576.
Genes (Basel). 2023.
PMID: 36980848
Free PMC article.
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Mutations in SCN3A cause early infantile epileptic encephalopathy.
Zaman T, Helbig I, Božović IB, DeBrosse SD, Bergqvist AC, Wallis K, Medne L, Maver A, Peterlin B, Helbig KL, Zhang X, Goldberg EM.
Zaman T, et al. Among authors: bozovic ib.
Ann Neurol. 2018 Apr;83(4):703-717. doi: 10.1002/ana.25188. Epub 2018 Mar 30.
Ann Neurol. 2018.
PMID: 29466837
Free PMC article.
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Altered LINE-1 Methylation in Mothers of Children with Down Syndrome.
Božović IB, Stanković A, Živković M, Vraneković J, Kapović M, Brajenović-Milić B.
Božović IB, et al.
PLoS One. 2015 May 27;10(5):e0127423. doi: 10.1371/journal.pone.0127423. eCollection 2015.
PLoS One. 2015.
PMID: 26017139
Free PMC article.
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Down syndrome: parental origin, recombination, and maternal age.
Vraneković J, Božović IB, Grubić Z, Wagner J, Pavlinić D, Dahoun S, Bena F, Culić V, Brajenović-Milić B.
Vraneković J, et al. Among authors: bozovic ib.
Genet Test Mol Biomarkers. 2012 Jan;16(1):70-3. doi: 10.1089/gtmb.2011.0066. Epub 2011 Aug 23.
Genet Test Mol Biomarkers. 2012.
PMID: 21861707
Free PMC article.
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MTHFR C677T and A1298C polymorphisms as a risk factor for congenital heart defects in Down syndrome.
Božović IB, Vraneković J, Cizmarević NS, Mahulja-Stamenković V, Prpić I, Brajenović-Milić B.
Božović IB, et al.
Pediatr Int. 2011 Aug;53(4):546-50. doi: 10.1111/j.1442-200X.2010.03310.x.
Pediatr Int. 2011.
PMID: 21159028
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