Found: 3
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Shedding light on the phenotypic–genotypic correlation of rare treatable and potentially treatable pediatric movement disorders.
- Published in:
- Egyptian Journal of Medical Human Genetics, 2022, v. 23, n. 1, p. 1, doi. 10.1186/s43042-022-00286-w
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- Article
The Diagnostic Value of Whole-Exome Sequencing in a Spectrum of Rare Neurological Disorders Associated with Cerebellar Atrophy.
- Published in:
- Molecular Neurobiology, 2024, v. 61, n. 8, p. 4949, doi. 10.1007/s12035-023-03866-y
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- Publication type:
- Article
The utility of exome sequencing in diagnosing pediatric neurodevelopmental disorders in a highly consanguineous population.
- Published in:
- Clinical Genetics, 2024, v. 106, n. 1, p. 82, doi. 10.1111/cge.14508
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- Article