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The utility of whole exome sequencing in diagnosing pediatric neurological disorders Cover

The utility of whole exome sequencing in diagnosing pediatric neurological disorders

Balkan Journal of Medical Genetics
Volume 23 (2020): Issue 2 (November 2020)
By: OY Muthaffar  
Open Access
|Mar 2021

Authors

OY Muthaffar

oymuthaffar@kau.edu.sa

Department of Pediatrics, King Abdulaziz University, Jeddah, Kingdom of Saudi Arabia
DOI: https://doi.org/10.2478/bjmg-2020-0028 | Journal eISSN: 2199-5761
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Language: English
Page range: 17 - 24
Published on: Mar 23, 2021
Published by: Macedonian Academy of Sciences and Arts
In partnership with: Paradigm Publishing Services
Publication frequency: 2 issues per year
Keywords:
Consanguinity,
Developmental delay,
Neurological disorders,
Saudi Arabia,
Whole exome sequencing (WES)
Related subjects:
Medicine,
Basic medical science,
Basic medical science, other

© 2021 OY Muthaffar, published by Macedonian Academy of Sciences and Arts
This work is licensed under the Creative Commons Attribution-NonCommercial-NoDerivatives 3.0 License.

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