Detection of mutations in the CYP21A2 gene: genotype-phenotype correlation in Slovenian couples with conceiving problems

por Stangler Herodež, Š, Fijavž, L, Zagradišnik, B, Kokalj Vokač, N
Publicado 2016

De Novo KMT2D Heterozygous Frameshift Deletion in a Newborn with a Congenital Heart Anomaly

por Stangler Herodež, Š, Marčun Varda, N, N, Kokalj Vokač, Krgović, D
Publicado 2020

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

MTHFR C677T and A1298C Genotypes and Haplotypes in Slovenian Couples with Unexplained Infertility Problems and in Embryonic Tissues from Spontaneous Abortions

por Stangler Herodež, Š, Zagradišnik, B, Erjavec Škerget, A, Zagorac, A, Takač, I, Vlaisavljević, V, Lokar, L, Kokalj Vokač, N
Publicado 201

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