نتائج البحث - Mario Ćuk

Innovative Genome Joint Analysis for identification of novel deep-intronic de novo pathogenic variants in KMT2A gene - WiedemannSteiner Syndrom حسب Matea Bagarić, Nives Živković Živković, Mario Ćuk

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Innovative Whole Genome Joint Analysis – case report of early diagnosis and preventive approach to HFE Hemochromatosis حسب Marjan Kulaš, Dina Gržan, Sandro Kukić, Luka Lovrenčić, Mario Ćuk

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Whole Genome Joint Analysis for identification of rare non-coding causative variants - case report of a child with mitochondrial disease حسب Dina Gržan, Marjan Kulaš, Lea Jukić, Petra Sulić, Mario Ćuk

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First Reported Case of Gabriele-de Vries Syndrome with Spinal Dysraphism حسب Nenad Koruga, Silvija Pušeljić, Marko Babić, Mario Ćuk, Andrea Cvitković Roić, Vjenceslav Vrtarić, Anamarija Soldo Koruga, Alen Rončević, Višnja Tomac, Tatjana Rotim, Tajana Turk, Domagoj Kretić, Nora Pušeljić, Rebeka Nađ, Ivana Serdarušić

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