De novo KMT2D heterozygous frameshift deletion in a newborn with a congenital heart anomaly von Stangler Herodež, Š, Marčun Varda, N, N, Kokalj Vokač, Krgović, D

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MTHFR C677T and A1298C Genotypes and Haplotypes in Slovenian Couples with Unexplained Infertility Problems and in Embryonic Tissues from Spontaneous Abortions von Stangler Herodež, S, Zagradišnik, B, Erjavec Škerget, A, Zagorac, A, Takač, I, Vlaisavljević, V, Lokar, L, Kokalj Vokač, N

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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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PB1939 ACCURACY AND SPEED OF REPORTING MOLECULAR RESPONSE IN PATIENTS ON TYROSINE KINASE INHIBITORS THERAPY WITH GENEXPERT CARTRIDGE‐BASED BCR‐ABL1 QUANTITATION von Dreisinger, M., Stangler Herodež, Š.

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The inhibitory effect of laughter yoga on the increase in postprandial blood glucose in type 2 diabetic patients von Cokolic, M, Herodez, S. Stangler, Sternad, S, Krebs, S

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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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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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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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