FMR1 gene mutations cause neurodevelopmental-degenerative disorders: Importance of fragile X testing in Serbia
nema
Main Authors: | Budimirovic Dejan B., Protic Dragana |
---|---|
Format: | Article |
Language: | English |
Published: |
Military Health Department, Ministry of Defance, Serbia
2016-01-01
|
Series: | Vojnosanitetski Pregled |
Subjects: | |
Online Access: | http://www.doiserbia.nb.rs/img/doi/0042-8450/2016/0042-84501600315B.pdf |
Similar Items
-
Drugs development and fragile X syndrome translational success story
by: Budimirović Dejan, et al.
Published: (2016-01-01) -
Neglected zoonosis: The prevalence of Salmonella spp. in pet reptiles in Serbia
by: Bošnjak Ivan, et al.
Published: (2016-01-01) -
Fragile X-Associated Disorders in Serbia: Baseline Quantitative and Qualitative Survey of Knowledge, Attitudes and Practices Among Medical Professionals
by: Dejan B. Budimirovic, et al.
Published: (2018-09-01) -
The Jankovic sisters’ legacy in the National library of Serbia
by: Prelić Mladena
Published: (2014-01-01) -
The state of research on church chant in medieval Serbia
by: Peno Vesna
Published: (2014-01-01)