Complex intrachromosomal rearrangement in 1q leading to 1q32.2 microdeletion: a potential role of SRGAP2 in the gyrification of cerebral cortex

nork Rincic, Martina, Rados, Milan, Krsnik, Zeljka, Gotovac, Kristina, Borovecki, Fran, Liehr, Thomas, Brecevic, Lukrecija
Argitaratua izan da Mol Cytogenet (2016)

Somatic Mosaicism in Cases with Small Supernumerary Marker Chromosomes

nork Liehr, Thomas, Karamysheva, Tatyana, Merkas, Martina, Brecevic, Lukrecija, Hamid, Ahmed B., Ewers, Elisabeth, Mrasek, Kristin, Kosyakova, Nadezda, Weise, Anja
Argitaratua 2010

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...

nork Brečević, Lukrecija, Rinčić, Martina, Krsnik, Željka, Sedmak, Goran, Hamid, Ahmed B., Kosyakova, Nadezda, Galić, Ivan, Liehr, Thomas, Borovečki, Fran
Argitaratua izan da Transl Neurosci (2015)