Mario Cuk
4PUBLICATIONS
8CO-AUTHORS
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Publications (4)
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|Feb 26, 2025
Novel TBR1 c.1303C>T Variant Led to Diagnosis of Intellectual Developmental Disorder with Autism and Speech Delay: Application of Comprehensive Family-Based Whole-Genome Analysis.Mario Ćuk, Busra Unal, Matea Bagarić
|Oct 26, 2024
Novel Variant in ANO5 Muscular Dystrophy: Identification by Whole Genome Sequencing and Quad Analysis.Mario Ćuk, Busra Unal, Luka Lovrenčić
|Sep 28, 2024
Novel RAI1:c.2736delC Variant in Smith-Magenis Syndrome: Identification by Whole Genome Sequencing and Joint Analysis.Mario Cuk, Busra Unal, Nives Jandric
|Jul 27, 2024
Diagnosis of Two Unrelated Syndromes of Prader-Willi and Calpainopathy: Insight from Trio Whole Genome Analysis and Isodisomy Mapping.Mario Cuk, Busra Unal, Andjela Bevanda
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