The Role of Next-Generation Sequencing in the Management of Patients with Suspected Non-Ischemic Cardiomyopathy after Syncope or Termination of Sudden Arrhythmic Death von Vokač, Damijan, Stangler Herodež, Špela, Krgović, Danijela, Kokalj Vokač, Nadja

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Impaired Neurodevelopmental Genes in Slovenian Autistic Children Elucidate the Comorbidity of Autism With Other Developmental Disorders von Krgovic, Danijela, Gorenjak, Mario, Rihar, Nika, Opalic, Iva, Stangler Herodez, Spela, Gregoric Kumperscak, Hojka, Dovc, Peter, Kokalj Vokac, Nadja

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Identification of potentially pathogenic variants for autism spectrum disorders using gene-burden analysis von Rihar, Nika, Krgovic, Danijela, Kokalj-Vokač, Nadja, Stangler-Herodez, Spela, Zorc, Minja, Dovc, Peter

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Identification of genomic copy number variations associated with specific clinical features of head and neck cancer von Zagradišnik, Boris, Krgović, Danijela, Herodež, Špela Stangler, Zagorac, Andreja, Ćižmarević, Bogdan, Vokač, Nadja Kokalj

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Slovenian five-year experiences with rapid prenatal diagnosis of common chromosome aneuploidies using quantitative-fluorescence polymerase chain reaction von Škerget, Alenka Erjavec, Herodež, Spela Stangler, Zagorac, Andreja, Zagradišnik, Boris, Mujezinović, Faris, Vokač, Nadja Kokalj

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Polymorphisms in four candidate genes in young patients with essential hypertension von MARCUN VARDA, Natasa, ZAGRADISNIK, Boris, STANGLER HERODEZ, Spela, KOKALJ VOKAC, Nadja, GREGORIC, Alojz

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Is the JAK2 V617F Mutation a Hallmark for Different Forms of Thrombosis? von Zerjavic, Katja, Zagradisnik, Boris, Stangler Herodez, Spela, Lokar, Lidija, Glaser Krasevac, Marjana, Kokalj Vokac, Nadja

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Detection of mutations in the CYP21A2 gene: genotype-phenotype correlation in Slovenian couples with conceiving problems von Herodez, Spela Stangler, Fijavz, L, Zagradisnik, B, Kokalj Vokac, N

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Solvent extraction study of antioxidants from Balm (Melissa officinalis L.) leaves von Herodež, Špela Stangler, Hadolin, Majda, Škerget, Mojca, Knez, Željko

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Molecular Diagnosis of PMP22 Gene Duplications and Deletions: Comparison of Different Methods von Herodež, Š Stangler, Zagradišnik, B, Škerget, A Erjavec, Zagorac, A, Vokač, N Kokalj

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Subtelomeric chromosome rearrangements in children with idiopathic mental retardation: applicability of three molecular-cytogenetic methods von Erjavec-Skerget, Alenka, Stangler-Herodez, Spela, Zagorac, Andreja, Zagradisnik, Boris, Kokalj-Vokac, Nadja

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Novosti – izkušnje – pobude – odmevi: zdravje in smeh med čustvi in geni von Simona Krebs, Špela Stangler Herodež

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Polymorphisms in four candidate genes in young patients with essential hypertension von Marčun Varda, Nataša, Zagradišnik, Boris, Stangler Herodež, Špela, Kokalj Vokač, Nadja, Gregorič, Alojz

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Subtelomeric Chromosome Rearrangements in Children with Idiopathic Mental Retardation: Applicability of Three Molecular-cytogenetic Methods von Erjavec-Škerget, Alenka, Stangler-Herodež, Špela, Zagorac, Andreja, Zagradišnik, Boris, Kokalj-Vokač, Nadja

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