Autori: Cuturilo Goran
| Naslov | Mowat-Wilson syndrome: growth charts (Meeting Abstract) |
| Autori | Ivanovski I ... Cuturilo Goran ... Kuburovic Vladimir ... (broj koautora 50) |
| Info | EUROPEAN JOURNAL OF HUMAN GENETICS, (2020), vol. 28 br. SUPPL 1, Suppl. 1, str. 471-473 |
| Ispravka | Web of Science Elečas Rang časopisa Citati: Web of Science Scopus |
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| Naslov | Mowat-Wilson syndrome: growth charts (Article) |
| Autori | Ivanovski Ivan P  Djuric Olivera S ... Cuturilo Goran ... Kuburovic Vladimir ... (broj koautora 53)
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| Info | ORPHANET JOURNAL OF RARE DISEASES, (2020), vol. 15 br. 1, str. - |
| Projekat | Telethon ItalyFondazione Telethon [GTB12001]; Associazione Italiana Mowat Wilson ONLUS [GTB12001] |
| Ispravka | Web of Science Članak Elečas Rang časopisa Citati: Web of Science Scopus |
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| Naslov | Diagnostic and Clinical Utility of Clinical Exome Sequencing in Children With Moderate and Severe Global Developmental Delay / Intellectual Disability (Article) |
| Autori | Ruml-Stojanovic Jelena Miletic Aleksandra Peterlin Borut Maver Ales Mijovic Marija Borlja Nikola Dimitrijevic Brankica Soldatovic Ivan A Cuturilo Goran
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| Info | JOURNAL OF CHILD NEUROLOGY, (2020), vol. 35 br. 2, str. 116-131 |
| Ispravka | Web of Science Članak Elečas Rang časopisa Citati: Web of Science Scopus |
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| Naslov | GLUT1 deficiency syndrome: a case report with a novel SLC2A1 mutation (Article) |
| Autori | Ivancevic Nikola Cerovac Natasa M Nikolic Blazo Cuturilo Goran Marjanovic Ana Marjanovic Ana Novakovic Ivana V
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| Info | VOJNOSANITETSKI PREGLED, (2019), vol. 76 br. 5, str. 543-546 |
| Projekat | Serbian Ministry of Education, Science and Technological Development [ON175091] |
| Ispravka | Web of Science Članak Elečas Rang časopisa Citati: Web of Science Scopus |
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| Naslov | Otopalatodigital Syndrome Type I: Novel Characteristics and Prenatal Manifestations in Two Siblings (Article) |
| Autori | Joksic Ivana D Cuturilo Goran Jurisic Aleksandar I Djuricic Slavisa M Peterlin Borut Mijovic Marija Karadzov-Orlic Natasa T Egic Amira Milovanovic Zagorka M
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| Info | BALKAN JOURNAL OF MEDICAL GENETICS, (2019), vol. 22 br. 2, str. 83-87 |
| Ispravka | Web of Science Članak Elečas Rang časopisa Citati: Web of Science Scopus |
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| Naslov | Clinical Next Generation Sequencing Reveals An H3f3a Gene as a New Potential Gene Candidate for Microcephaly Associated with Severe Developmental Delay, Intellectual Disability and Growth Retardation (Article) |
| Autori | Maver Ales Cuturilo Goran Stojanovic Ruml J Peterlin Borut |
| Info | BALKAN JOURNAL OF MEDICAL GENETICS, (2019), vol. 22 br. 2, str. 65-68 |
| Projekat | Slovenian Research Agency - Slovenia [J3-8205, J3-9280, P3-0326] |
| Ispravka | Web of Science Članak Elečas Rang časopisa Citati: Web of Science Scopus |
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| Naslov | Rare missense TUBGCP5 gene variant in a patient with primary microcephaly (Article) |
| Autori | Maver Ales Cuturilo Goran Kovanda Anja Miletic Aleksandra Peterlin Borut |
| Info | EUROPEAN JOURNAL OF MEDICAL GENETICS, (2019), vol. 62 br. 12, str. - |
| Projekat | ARRS research programme [P3-0326, J3-8205, J3-5506] |
| Ispravka | Web of Science Članak Elečas Rang časopisa Citati: Web of Science Scopus |
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| Naslov | Phenotypic overlap between spondyloepimetaphyseal dysplasia with joint laxity type 2 and Morquio syndrome type A: case report (Meeting Abstract) |
| Autori | Mijovic Marija Miletic Aleksandra Janeski Hristina Dimitrijevic Brankica Ruml-Stojanovic Jelena Lukic M Cuturilo Goran |
| Info | EUROPEAN JOURNAL OF HUMAN GENETICS, (2019), vol. 27 br. , Suppl. 2, str. 1299-1300 |
| Ispravka | Web of Science Elečas Rang časopisa Citati: Web of Science |
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| Naslov | Novel mosaic CREBBP mutation in a patient with overlapping clinical features of Rubinstein-Taybi syndrome and Floating-Harbor syndrome (Meeting Abstract) |
| Autori | Ruml-Stojanovic Jelena Mijovic Marija Miletic Aleksandra Dimitrijevic Brankica Peterlin Borut Maver Ales Cuturilo Goran |
| Info | EUROPEAN JOURNAL OF HUMAN GENETICS, (2019), vol. 27 br. , Suppl. 1, str. 945-945 |
| Ispravka | Web of Science Elečas Rang časopisa Citati: Web of Science |
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| Naslov | The patient with fragile site on chromosome 16 and four missed abortions : a case report (Meeting Abstract) |
| Autori | Komnenic-Radovanovic Milica Petrovic Bojana Dencic-Fekete Marija Jovanovic Jelica V Djordjevic Vesna R Cuturilo Goran Dimitrijevic B Miletic A Ruml-Stojanovic Jelena Radovanovic M Kontic-Vucinic Olivera |
| Info | EUROPEAN JOURNAL OF HUMAN GENETICS, (2019), vol. 27 br. , Suppl. 1, str. 875-876 |
| Ispravka | Web of Science Elečas Rang časopisa Citati: Web of Science |
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