Literature DB >> 29341564

FMR1 gene mutations cause neurodevelopmental-degenerative disorders: Importance of fragile X testing in Serbia

Dejan B Budimirovic, Dragana Protic.   

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Year:  2016        PMID： 29341564     DOI： 10.2298/VSP161006315B

Source DB:  PubMed          Journal:  Vojnosanit Pregl        ISSN： 0042-8450            Impact factor:   0.168


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  2 in total

1.  Raising Knowledge and Awareness of Fragile X Syndrome in Serbia, Georgia, and Colombia: A Model for Other Developing Countries?

Authors:  Dragana Protic; Maria Jimena Salcedo-Arellano; Maja Stojkovic; Wilmar Saldarriaga; Laura Alejandra Ávila Vidal; Robert M Miller; Nazi Tabatadze; Marina Peric; Randi Hagerman; Dejan B Budimirovic
Journal:  Yale J Biol Med       Date:  2021-12-29

2.  Fragile X-Associated Disorders in Serbia: Baseline Quantitative and Qualitative Survey of Knowledge, Attitudes and Practices Among Medical Professionals.

Authors:  Dejan B Budimirovic; Smiljana Cvjetkovic; Zoran Bukumiric; Phan Q Duy; Dragana Protic
Journal:  Front Neurosci       Date:  2018-09-21       Impact factor: 4.677
  2 in total

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