9 results on '"Chatron N."'
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2. Severe cognitive impairment and early-onset epilepsy in six patients with the de novo p.Glu590Lys variant of CUX2
3. Three new cases of asparagine synthetase deficiency: Confirmation of a poor neurological outcome and a new molecular mechanism
4. West syndrome due to compound heterozygous QARS mutations
5. Next-generation sequencing allows a diagnostic yield of 23.7% in monogenic epilepsies
6. Christianson syndrome: An underestimated cause of electrical status epilepticus in sleep?
7. Next-generation sequencing (NGS) is a powerful tool to improve diagnostic yield in intellectual disability
8. Prenatal microarray comparative genomic hybridization: Experience from the two first years of activity at the Lyon university-hospital
9. Study of six patients with complete F9 deletion characterized by cytogenetic microarray: role of the SOX3 gene in intellectual disability
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