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

Por Rincic, Martina, Rados, Milan, Krsnik, Zeljka, Gotovac, Kristina, Borovecki, Fran, Liehr, Thomas, Brecevic, Lukrecija
Publicado no Mol Cytogenet (2016)

Somatic Mosaicism in Cases with Small Supernumerary Marker Chromosomes

Por Liehr, Thomas, Karamysheva, Tatyana, Merkas, Martina, Brecevic, Lukrecija, Hamid, Ahmed B., Ewers, Elisabeth, Mrasek, Kristin, Kosyakova, Nadezda, Weise, Anja
Publicado em 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...

Por Brečević, Lukrecija, Rinčić, Martina, Krsnik, Željka, Sedmak, Goran, Hamid, Ahmed B., Kosyakova, Nadezda, Galić, Ivan, Liehr, Thomas, Borovečki, Fran
Publicado no Transl Neurosci (2015)