Autori: Cuturilo Goran
| Naslov | The clinical significance ofA2ML1variants in Noonan syndrome has to be reconsidered (Article) |
| Autori | Brinkmann Julia ... Cuturilo Goran ... (broj koautora 25) |
| Info | EUROPEAN JOURNAL OF HUMAN GENETICS, (2021), vol. 29 br. 3, str. 524-527 |
| Projekat | ERN-ITHACA networking; German Federal Ministry of Education and Research-BMBF (German Network for RASopathy Research "GeNeRARe") [FKZ: 01GM1519A]; German Federal Ministry of Education and Research-BMBF (European Joint Programme on Rare Diseases (NSEuroNet |
| Ispravka | Web of Science Članak Elečas Rang časopisa Citati: Web of Science |
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| Naslov | Rare Pathogenic Copy Number Variation in the 16p11.2 (BP4-BP5) Region Associated with Neurodevelopmental and Neuropsychiatric Disorders: A Review of the Literature (Review) |
| Autori | Oliva-Teles Natalia De Stefano Maria Chiara Gallagher Louise Rakic Severin Jorge Paula Cuturilo Goran Markovska-Simoska Silvana Borg Isabella Wolstencroft Jeanne Tumer Zeynep Harwood Adrian J Kodra Yllka Skuse David |
| Info | INTERNATIONAL JOURNAL OF ENVIRONMENTAL RESEARCH AND PUBLIC HEALTH, (2020), vol. 17 br. 24, str. - |
| Projekat | COST ACTIONEuropean Cooperation in Science and Technology (COST) [16210] |
| Ispravka | Web of Science Članak Elečas Rang časopisa Citati: Web of Science Scopus |
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| Naslov | Skeletal dysplasia in the era of genomic testing: first experience of a single genetic outpatient clinic from Serbia (Meeting Abstract) |
| Autori | Mijovic Marija  Ruml-Stojanovic Jelena Miletic Aleksandra Bosankic Brankica Janeski Hristina Peterlin Borut Maver Ales Cuturilo Goran
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| Info | EUROPEAN JOURNAL OF HUMAN GENETICS, (2020), vol. 28 br. SUPPL 1, Suppl. 1, str. 831-831 |
| Ispravka | Web of Science Elečas Rang časopisa Citati: Web of Science |
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| Naslov | Recurrent congenital microcephaly: a case report (Meeting Abstract) |
| Autori | Komnenic-Radovanovic Milica Novakovic Ivana V Cuturilo Goran Ruml-Stojanovic Jelena Petrovic Bojana Kontic-Vucinic Olivera
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| Info | EUROPEAN JOURNAL OF HUMAN GENETICS, (2020), vol. 28 br. SUPPL 1, Suppl. 1, str. 801-802 |
| Ispravka | Web of Science Elečas Rang časopisa Citati: Web of Science |
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| Naslov | The role of A2ML1 variants in Noonan syndrome remains unverified (Meeting Abstract) |
| Autori | Brinkmann Julia ... Cuturilo Goran ... (broj koautora 24) |
| Info | EUROPEAN JOURNAL OF HUMAN GENETICS, (2020), vol. 28 br. SUPPL 1, Suppl. 1, str. 479-479 |
| Ispravka | Web of Science Elečas Rang časopisa Citati: Web of Science |
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| 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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