Specific behavioural phenotype and secondary cognitive decline as a result of an 8.6 Mb deletion of 2q32.2q33.1

por Gregoric Kumperscak, Hojka, Krgovic, Danijela, Vokac, Nadja Kokalj
Publicado 2016

Submicroscopic interstitial deletion of chromosome 11q22.3 in a girl with mild mental retardation and facial dysmorphism: Case report

por Krgovic, Danijela, Marcun Varda, Natasa, Zagorac, Andreja, Kokalj-Vokac, Nadja
Publicado 2011

Rare structural variants in the DOCK8 gene identified in a cohort of 439 patients with neurodevelopmental disorders

por Krgovic, Danijela, Kokalj Vokac, Nadja, Zagorac, Andreja, Gregoric Kumperscak, Hojka
Publicado 2018

A coalescence of two syndromes in a girl with terminal deletion and inverted duplication of chromosome 5

por Krgovic, Danijela, Blatnik, Ana, Burmas, Ante, Zagorac, Andreja, Kokalj Vokac, Nadja
Publicado 2014

Identification of potentially pathogenic variants for autism spectrum disorders using gene-burden analysis

por Rihar, Nika, Krgovic, Danijela, Kokalj-Vokač, Nadja, Stangler-Herodez, Spela, Zorc, Minja, Dovc, Peter
Publicado 2023

Identification of genomic copy number variations associated with specific clinical features of head and neck cancer

por Zagradišnik, Boris, Krgović, Danijela, Herodež, Špela Stangler, Zagorac, Andreja, Ćižmarević, Bogdan, Vokač, Nadja Kokalj
Publicado 2018

CNVs and Chromosomal Aneuploidy in Patients With Early-Onset Schizophrenia and Bipolar Disorder: Genotype-Phenotype Associations

por Gregoric Kumperscak, Hojka, Krgovic, Danijela, Drobnic Radobuljac, Maja, Senica, Nina, Zagorac, Andreja, Kokalj Vokac, Nadja
Publicado 2021

Impaired Neurodevelopmental Genes in Slovenian Autistic Children Elucidate the Comorbidity of Autism With Other Developmental Disorders

por Krgovic, Danijela, Gorenjak, Mario, Rihar, Nika, Opalic, Iva, Stangler Herodez, Spela, Gregoric Kumperscak, Hojka, Dovc, Peter, Kokalj Vokac, Nadja
Publicado 2022