14 results on '"Sadat, Roa"'
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2. Edematous severe acute malnutrition is characterized by hypomethylation of DNA
3. P285: Genetic testing strategies for rare and undiagnosed neurogenetic conditions: Utilization of exome sequencing, metabolic, and panel testing
4. Genetic Testing and Counseling and Child Neurology
5. Increased parental anxiety and a benign clinical course: Infants identified with short-chain acyl-CoA dehydrogenase deficiency and isobutyryl-CoA dehydrogenase deficiency through newborn screening in Georgia.
6. Functional cellular analyses reveal energy metabolism defect and mitochondrial DNA depletion in a case of mitochondrial aconitase deficiency.
7. eP226: Dual diagnoses in neurogenetics- A case series of pediatric movement disorders and clinical management
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