Integrative ‘Omic’ Approach Towards Understanding the Nature of Human Diseases by Peterlin Borut, Maver A

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Clinical next generation sequencing reveals an H3F3A gene as a new potential gene candidate for microcephaly associated with severe developmental delay, intellectual disability and... by Maver A, Čuturilo G, Ruml Stojanović J, Peterlin B

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Family history as an important factor for stratifying participants in genetic studies of major depression by Zalar B, Blatnik A, Maver A, Klemenc-Ketiš Z, Peterlin B

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Polymorphism of the ADRB2 rs1042713 gene is not associated with spontaneous preterm birth: Analyses in a Slovenian sample and meta analysis by Peterlin A, Maver A, Jan Z, Lovrecic L, Tul N, Peterlin B

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Sensorineural Hearing Loss in a Child with Succinic Semialdehyde Dehydrogenase Deficiency by Parezanović M, Ilić N, Ostojić S, Stevanović G, Ječmenica J, Maver A, Sarajlija A

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A novel likely pathogenic variant in the RUNX1 gene as the cause of congenital thrombocytopenia by Despotović M, Pereza N, Peterlin B, Ostojić S, Golob B, Maver A, Roganović J

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Expanding the Phenotypic Spectrum: Chronic Kidney Disease in a Patient with Combined Oxidative Phosphorylation Defect 21 by Paripović A, Maver A, Stajić N, Putnik J, Ostojić S, Alimpić B, Ilić N, Sarajlija A

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A novel variant in the LIPA gene associated with distinct phenotype by Sarajlija A., Armengol L., Maver A., Kitic I., Prokic D., Cehic M., Djuricic M.S., Peterlin B.

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Clinical Experience of Neurological Mitochondrial Diseases in Children and Adults: A Single-Center Study by Rogac M, Neubauer D, Leonardis L, Pecaric N, Meznaric M, Maver A, Sperl W, Garavaglia BM, Lamantea E, Peterlin B

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