Autori: Maric Nina
Naslov | Novel deep intronic variant in GALC gene in the patient with infantile Krabbe disease (Meeting Abstract) |
Autori | Maric Nina Kecman Bozica Ostojic Slavica B |
Info | EUROPEAN JOURNAL OF HUMAN GENETICS, (2024), vol. 32 br. , Suppl. 2, str. 1030-1031 |
Ispravka | ISI/Web of Science Elečas Rang časopisa |
Naslov | Novel deep intronic variant in GALC gene in the patient with infantile Krabbe disease (Meeting Abstract) |
Autori | Maric Nina Kecman Bozica Ostojic Slavica B |
Info | EUROPEAN JOURNAL OF HUMAN GENETICS, (2024), vol. 32 br. , Suppl. 2, str. 1030-1031 |
Ispravka | ISI/Web of Science Elečas Rang časopisa |
Naslov | Noonan Syndrome: Relation of Genotype to Cardiovascular Phenotype-A Multi-Center Retrospective Study (Article) |
Autori | Ilic Nikola A Krasic Stasa D Maric Nina Gasic Vladimir V Krstic Jovana Cvetkovic Dimitrije Miljkovic Vesna Zec Boris Maver Ales Vukomanovic Vladislav A Sarajlija Adrijan |
Info | GENES, (2024), vol. 15 br. 11, str. - |
Ispravka | ISI/Web of Science Članak Elečas Rang časopisa |
Naslov | Reverse Phenotyping after Whole-Exome Sequencing in Children with Developmental Delay/Intellectual Disability-An Exception or a Necessity? (Article) |
Autori | Ilic Nikola A Maric Nina ... Kravljanac Ruzica M Cirkovic Jana Krstic Jovana Radivojevic Danijela Cirkovic Sanja S Ostojic Slavica B Krasic Stasa D Paripovic Aleksandra Vukomanovic Vladislav A ... Maric Gorica D Sarajlija Adrijan |
Info | GENES, (2024), vol. 15 br. 6, str. - |
Ispravka | ISI/Web of Science Članak Elečas Rang časopisa |
Naslov | The importance of comprehensive genomic profiling in differential diagnosis and discovery of novel disease causing genetic variants in patients with pediatric lung diseases (Meeting Abstract) |
Autori | Andjelkovic Marina Z Minic Predrag B Vreca Misa Stojiljkovic Maja M Skakic Anita G Sovtic Aleksandar D Rodic Milan Skodric-Trifunovic Vesna D Maric Nina Visekruna Jelena Spasovski Vesna M Pavlovic Sonja T |
Info | EUROPEAN JOURNAL OF HUMAN GENETICS, (2019), vol. 27 br. , Suppl. 1, str. 89-90 |
Ispravka | ISI/Web of Science Elečas Rang časopisa Citati: ISI/Web of Science |
Naslov | Genomic profiling supports the diagnosis of primary ciliary dyskinesia and reveals novel candidate genes and genetic variants (Article) |
Autori | Andjelkovic Marina Z Minic Predrag B Vreca Misa Stojiljkovic Maja M Skakic Anita G Sovtic Aleksandar D Rodic Milan Skodric-Trifunovic Vesna D Maric Nina Visekruna Jelena Spasovski Vesna M Pavlovic Sonja T |
Info | PLOS ONE, (2018), vol. 13 br. 10, str. - |
Projekat | Ministry of Education, Science and Technological Development, Republic of Serbia [III 41004] |
Ispravka | ISI/Web of Science Članak Elečas Rang časopisa Citati: ISI/Web of Science Scopus |