Autori: Djuranovic Ana S
Naslov | Enrichment of pathogenic copy number variants on 17q chromosome in patients with skeletal findings (Meeting Abstract) |
Autori | Perovic Dijana ![]() ![]() ![]() ![]() ![]() ![]() ![]() |
Info | EUROPEAN JOURNAL OF HUMAN GENETICS, (2024), vol. 32 br. , Suppl. 2, str. 1384-1385 |
Ispravka | Web of Science Elečas Rang časopisa |
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Naslov | Chromosomal microarray analysis in children with syndromic short stature (Meeting Abstract) |
Autori | Maksimovic Nela S ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() |
Info | EUROPEAN JOURNAL OF HUMAN GENETICS, (2024), vol. 32 br. , Suppl. 2, str. 1115-1115 |
Ispravka | Web of Science Elečas Rang časopisa |
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Naslov | Diagnostic yield of chromosomal microarray analysis in patients with congenital heart disease (Meeting Abstract) |
Autori | Damnjanovic Tatjana M ![]() ![]() ![]() ![]() ![]() ![]() ![]() |
Info | EUROPEAN JOURNAL OF HUMAN GENETICS, (2024), vol. 32 br. , Suppl. 2, str. 1018-1018 |
Ispravka | Web of Science Elečas Rang časopisa |
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Naslov | Enrichment of pathogenic copy number variants on 17q chromosome in patients with skeletal findings (Meeting Abstract) |
Autori | Perovic Dijana ![]() ![]() ![]() ![]() ![]() ![]() ![]() |
Info | EUROPEAN JOURNAL OF HUMAN GENETICS, (2024), vol. 32 br. , Suppl. 2, str. 1384-1385 |
Ispravka | Web of Science Elečas Rang časopisa |
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Naslov | Chromosomal microarray analysis in children with syndromic short stature (Meeting Abstract) |
Autori | Maksimovic Nela S ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() |
Info | EUROPEAN JOURNAL OF HUMAN GENETICS, (2024), vol. 32 br. , Suppl. 2, str. 1115-1115 |
Ispravka | Web of Science Elečas Rang časopisa |
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Naslov | Diagnostic yield of chromosomal microarray analysis in patients with congenital heart disease (Meeting Abstract) |
Autori | Damnjanovic Tatjana M ![]() ![]() ![]() ![]() ![]() ![]() ![]() |
Info | EUROPEAN JOURNAL OF HUMAN GENETICS, (2024), vol. 32 br. , Suppl. 2, str. 1018-1018 |
Ispravka | Web of Science Elečas Rang časopisa |
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Naslov | Three case reports of patients with rare copy number variations in the recurrent 2q11.1-q11.2 region (Meeting Abstract) |
Autori | Perovic Dijana ![]() ![]() ![]() ![]() ![]() |
Info | EUROPEAN JOURNAL OF HUMAN GENETICS, (2023), vol. 31 br. , Suppl. 1, str. 267-268 |
Ispravka | Web of Science Elečas Rang časopisa |
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Naslov | Study of IL6 and TNF genes polymorphisms as a risk factor for the development of early neurological disorders and subsequent consequences in neonates (Meeting Abstract) |
Autori | Djuranovic Ana S ![]() ![]() ![]() ![]() |
Info | EUROPEAN JOURNAL OF HUMAN GENETICS, (2023), vol. 31 br. , Suppl. 1, str. 171-171 |
Ispravka | Web of Science Elečas Rang časopisa |
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Naslov | Chromosomal microarray in postnatal diagnosis of congenital anomalies and neurodevelopmental disorders in Serbian patients (Article) |
Autori | Perovic Dijana ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() |
Info | JOURNAL OF CLINICAL LABORATORY ANALYSIS, (2022), vol. 36 br. 6, str. - |
Projekat | Ministarstvo Prosvete, Nauke i Tehnoloskog Razvoja [175091] |
Ispravka | Web of Science Članak Elečas Rang časopisa Citati: Web of Science Scopus |
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Naslov | Polymorphisms in genes for proinflammatory cytokines IL-6, IL-1 ss, andTNF-alpha in relation with Parkinson's disease progression (Meeting Abstract) |
Autori | Pesic Milica ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() |
Info | EUROPEAN JOURNAL OF HUMAN GENETICS, (2020), vol. 28 br. SUPPL 1, Suppl. 1, str. 888-888 |
Ispravka | Web of Science Elečas Rang časopisa Citati: Web of Science |
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