Altered LINE-1 Methylation in Mothers of Children with Down Syndrome von Babic Bozovic, Ivana, Kapovic, Miljenko, Brajenovic-Milic, Bojana, Vranekovic, Jadranka, Zivkovic, Maja, Stankovic, Aleksandra

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Methylenetetrahydrofolate Reductase Dimer Configuration as a Risk Factor for Maternal Meiosis I-Derived Trisomy 21 von Vraneković, Jadranka, Babić Božović, Ivana, Bilić Čače, Iva, Brajenović Milić, Bojana

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Diagnostic yield of exome sequencing in myopathies: Experience of a Slovenian tertiary centre von Babić Božović, Ivana, Maver, Aleš, Leonardis, Lea, Meznaric, Marija, Osredkar, Damjan, Peterlin, Borut

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Mutations in SCN3A cause early infantile epileptic encephalopathy von Zaman, Tariq, Helbig, Ingo, Božović, Ivana Babić, DeBrosse, Suzanne D., Bergqvist, A. Christina, Wallis, Kimberly, Medne, Livija, Maver, Aleš, Peterlin, Borut, Helbig, Katherine L., Zhang, Xiaohong, Goldberg, Ethan M.

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Maternal LINE-1 DNA Methylation and Congenital Heart Defects in Down Syndrome von Babić Božović, Ivana, Stanković, Aleksandra, Živković, Maja, Vraneković, Jadranka, Mahulja-Stamenković, Vesna, Brajenović-Milić, Bojana

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Streamlined two‐step fragment analysis PCR and exome sequencing of RFC1 for diagnostic testing of suspected CANVAS patients von Jaklič, Helena, Božović, Ivana Babič, Peterlin, Borut, Kovanda, Anja

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MTHFR C677T and A1298C polymorphisms as a risk factor for congenital heart defects in Down syndrome von Babic Bozovic, Ivana, Vranekovic, Jadranka, StarcevicCizmarevic, Nada, Mahulja-Stamenkovic, Vesna, Prpic, Igor, Brajenovic-Milic, Bojana

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Evaluation of Optical Genome Mapping in Clinical Genetic Testing of Facioscapulohumeral Muscular Dystrophy von Kovanda, Anja, Lovrečić, Luca, Rudolf, Gorazd, Babic Bozovic, Ivana, Jaklič, Helena, Leonardis, Lea, Peterlin, Borut

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DNMT3B rs2424913 as a Risk Factor for Congenital Heart Defects in Down Syndrome von Majstorović, Dijana, Barišić, Anita, Božović, Ivana Babić, Čače, Iva Bilić, Čače, Neven, Štifanić, Mauro, Vraneković, Jadranka

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Functional inference of methylenetetrahydrofolate reductase gene polymorphisms on enzyme stability as a potential risk factor for Down syndrome in Croatia von Vraneković, Jadranka, Babić Bozović, Ivana, Starcević Cizmarević, Nada, Buretić-Tomljanović, Alena, Ristić, Smiljana, Petrović, Oleg, Kapović, Miljenko, Brajenović-Milić, Bojana

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The Expanding Phenotypical Spectrum of WARS2 -Related Disorder: Four Novel Cases with a Common Recurrent Variant von Pauly, Martje G, Korenke, G Christoph, Diaw, Sokhna Haissatou, Grözinger, Anne, Cazurro-Gutiérrez, Ana, Pérez-Dueñas, Belén, González, Victoria, Macaya, Alfons, Serrano Antón, Ana Teresa, Peterlin, Borut, Božović, Ivana Babić, Maver, Aleš, Münchau, Alexander, Lohmann, Katja

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Čimbenici rizika za javljanje intraventrikularnog krvarenja u prijevremeno rođene novorođenčadi u Jedinici novorođenačkog intenzivnog liječenja, Klinike za ginekologiju i porodništ... von Bilić Čače, Iva, Milardović, Ana, Babić Božović, Ivana, Kolak, Maja

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Folati i folna kiselina: dosadašnje spoznaje von Babić Božović, Ivana, Vraneković, Jadranka

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Functional inference of methylenetetrahydrofolate reductase gene polymorphisms on enzyme stability as a potential risk factor for Down syndrome in Croatia von Vraneković, Jadranka, Babić Bozović, Ivana, Starcević Cizmarević, Nada, Buretić-Tomljanović, Alena, Ristić, Smiljana, Petrović, Oleg, Kapović, Miljenko, Brajenović-Milić, Bojana

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IDNMT3B/I rs2424913 as a Risk Factor for Congenital Heart Defects in Down Syndrome von Majstorović, Dijana, Barišić, Anita, Božović, Ivana Babić, Čače, Iva Bilić, Čače, Neven, Štifanić, Mauro, Vraneković, Jadranka

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The Expanding Phenotypical Spectrum of IWARS2/I-Related Disorder: Four Novel Cases with a Common Recurrent Variant von Pauly, Martje G, Korenke, G. Christoph, Diaw, Sokhna Haissatou, Grözinger, Anne, Cazurro-Gutiérrez, Ana, Pérez-Dueñas, Belén, González, Victoria, Macaya, Alfons, Serrano Antón, Ana Teresa, Peterlin, Borut, Božović, Ivana Babić, Maver, Aleš, Münchau, Alexander, Lohmann, Katja

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Down syndrome: parental origin, recombination, and maternal age von Vraneković, Jadranka, Božović, Ivana Babić, Grubić, Zorana, Wagner, Jasenka, Pavlinić, Dinko, Dahoun, Sophie, Bena, Frédérique, Culić, Vida, Brajenović-Milić, Bojana

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The Expanding Phenotypical Spectrum of WARS2 -Related Disorder : Four Novel Cases with a Common Recurrent Variant von Pauly, Martje G, Korenke, G. Christoph, Diaw, Sokhna Haissatou, Grözinger, Anne, Cazurro-Gutiérrez, Ana Laura, Pérez-Dueñas, Belén, González, Victoria, Macaya Ruiz, Alfons, Serrano Antón, Ana Teresa, Peterlin, Borut, Božović, Ivana Babić, Maver, Aleš, Münchau, Alexander, Lohmann, Katja, Universitat Autònoma de Barcelona

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Risk factors of intraventricular hemorrhage in preterm infants in the Neonatal Intensive Care Unit , University Department of Obstetrics and Gynecology, University Hospital Center... von Bilić Čače, Iva, Milardović, Ana, Babić Božović, Ivana, Kolak, Maja

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Altered LINE-1 Methylation in Mothers of Children with Down Syndrome: e0127423 von Bozovic, Ivana Babic, Stankovic, Aleksandra, Zivkovic, Maja, Vranekovic, Jadranka, Kapovic, Miljenko, Brajenovic-Milic, Bojana

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