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Slika profila

Lukrecija Brečević

18566

Lukrecija

Brečević

dr. sc.

Naziv Uloga Akcije
MOLEKULARNA CITOGENETIKA U EVALUACIJI MENTALNE RETARDACIJE NEPOZNATE ETIOLOGIJE voditelj
Naziv Akcije
Rinčić, Martina ; Kopić, Janja ; Jakšić, Boris ; Krsnik, Željka ; Borovečki, Fran ; Brečević, Lukrecija Evolutionary novel genes in neurodevelopmental disorders // MNS Full Proceedings. 2022. str. 159-159
Rinčić, Martina ; Radoš, Milan ; Krsnik, Zeljka ; Liehr, Thomas ; Brecevic, Lukrecija Microdeletion of 7p21.3 and 12p13.32 in a female patient with severe microcephaly // 6th Belgian Brain Congress : abstracts ; u: Frontiers. 2016
Rincic, Martina ; Rados, Milan ; Krsnik, Zeljka ; Gotovac, Kristina ; Borovecki, Fran ; Liehr, Thomas ; Brecevic, Lukrecija Complex intrachromosomal rearrangement in 1q leading to 1q32.2 microdeletion: a potential role of SRGAP2 in the gyrification of cerebral cortex // Molecular Cytogenetics, 9 (2016), 19--. doi: 10.1186/s13039-016-0221-4
Rincic, Martina ; Rados, Milan ; Krsnik, Zeljka ; Gotovac, Kristina ; Nelle H ; Liehr, Thomas ; Borovecki, Fran ; Brecevic, Lukrecija Complex intrachromosomal rearrangement in 1q leading to 1q32.2 microdeletion: a potential role of SRGAP2 in the gyrification of cerebral cortex. 2015
Rinčić Martina ; Krsnik Željka ; Gotovac Kristina ; Liehr Thomas ; Borovecki Fran ; Brecevic Lukrecija Customized high resolution arrayCGH for neurodevelopmental disorders: our experience. 2015
Brečević, Lukrecija ; Rinčić, Martina ; Krsnik, Željka ; Sedmak, Goran ; Hamid, Ahmed B. ; Kosyakova, Nadezda ; Galić, Ivan ; Liehr, Thomas ; Borovečki, Fran Association of new deletion/duplication region at chromosome 1p21 with intellectual disability, severe speech deficit and autism spectrum disorder-like behavior: an all-in approach to solving the DPYD enigma // Translational Neuroscience, 6 (2015), 1; 59-86. doi: 10.1515/tnsci-2015-0007
Rinčić Martina ; Krsnik Željka ; Sedmak Goran ; Ahmed B. Hamid ; Galić Ivan ; Borovečki Fran ; Liehr Thomas ; Brečević Lukerecija Neurodevelopmental genes in new microdeletion/microduplication region in chromosome 1p21. 2015
Guilherme RS ; Klein E ; Hamid AB, Bhatt S ; Volleth M ; Polityko A ; Kulpanovich A ; Dufke A ; , AlbrechtB ; Morlot S ; Brečevic Lukrecija et al. HUMAN RING CHROMOSOMES – NEW INSIGHTS FOR THEIR CLINICAL SIGNIFICANCE // Balkan Journal of Medical Genetics, 16 (2013), 1; 13-19
Škrlec, Ivana ; Wagner, Jasenka ; Merkeš, Martina ; Pušeljić, Silvija ; Heffer, Marija ; Brečević, Lukrecija ; Liehr, Thomas De novo case of 3p deletion syndrome // Chromosome research. 2013. str. S47-S47
Merkaš, Martina ; Gotovac, Kristina ; Brečević, Lukrecija ; Borovečki, Fran ; Liehr, Thomas Evaluation of chromosomal mosaicism by aCGH and MLPA:molecular characterization of mosaic ring chromosome 22. // XII Russian Federation Congress “Modern technologies in pediatrics and pediatric surgery”, Moscow, Russia, 2013. 2013. str. 82-x
nije evidentirano
Naziv Uloga Akcije
Genetic diagnostics of intellectual disability disorder, autism spectrum disorder and epilepsy izumitelj/i