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Naslov Insight into Haploinsufficiency of the ERBB4 Gene: Expanding the Spectrum of Associated Phenotypes (Article; Early Access)
Autori Mademont-Soler Irene  ...  Perovic Dijana  ...  Kravljanac Ruzica M  ...  Bosankic Brankica  ...  Maksimovic Nela S  ...  (broj koautora 37) 
Info JOURNAL OF AUTISM AND DEVELOPMENTAL DISORDERS, (2026), vol. br. , str. -
Projekat Fundaci Instituci dels Centres de Recerca de Catalunya (CERCA)
Ispravka ISI/Web of Science   Članak   Elečas   Rang časopisa   Citati:
Naslov A Novel 4.2 kb deletion of the 3′UTR of RUNX2 Gene Causes Cleidocranial Dysplasia: Further Delineation of the Role of yhe 3′UTR (Article)
Autori Mijovic Marija  Cuturilo Goran  Ruml-Stojanovic Jelena  Brankovic Marija  Miletic A  Bosankic Brankica  Dedovic Maja  Perovic D  Maksimovic N  Damnjanovic Tatjana M 
Info BALKAN JOURNAL OF MEDICAL GENETICS, (2025), vol. 28 br. 2, str. 107-112
Ispravka ISI/Web of Science   Članak   Elečas   Rang časopisa  
Naslov Genetic evaluation of newborns with critical congenital heart defects admitted to the intensive care unit (Article)
Autori Miletic Aleksandra  Ruml-Stojanovic Jelena  Parezanovic Vojislav M  Rsovac Snezana  Drakulic Danijela D  Soldatovic Ivan A  Mijovic Marija  Bosankic Brankica  Petrovic Hristina  Borlja Nikola  Milivojevic Milena C  Marjanovic Ana  Marjanovic Ana  Cuturilo Goran 
Info EUROPEAN JOURNAL OF PEDIATRICS, (2021), vol. 180 br. 10, str. 3219-3227
Projekat Ministry of Education, Science and Technological Development, Republic of Serbia [451-03-68/2020-14/200042]
Ispravka ISI/Web of Science   Članak   Elečas   Rang časopisa   Citati: ISI/Web of Science   Scopus  
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