SciELO - Brasil - Epilepsy and ring chromosome 20: case report Epilepsy and ring chromosome 20: case report
Ring 22 QFNW French.pub - Unique - The Rare Chromosome ...
Ring chromosome 20 syndrome: Updates
Ring chromosome 20 syndrome with intractable epilepsy
Electroclinical evolution in ring chromosome 20 epilepsy syndrome: A case with severe phenotypic features followed for 25 years
Ring Chromosome 20 Syndrome | Semantic Scholar
Chromosome 20 - Wikipedia
John Libbey Eurotext - Epilepsies - Ring chromosome 20 and epilepsy: diversity of seizures presented by the patients as studied in video-EEG study. Is a subcortical dysfunctionning mainly involved in the epileptogenesis?
Ring 20 chromosome in a child with seizures, minor anomalies, and retardation. - Abstract - Europe PMC
Ring Chromosome 20 with Nonconvulsive Status Epilepticus: Electroclinical Correlation of a Rare Epileptic Syndrome - Chaichon Locharernkul, Alois Ebner, Chinvorn Promchainant, 2005
Ring Chromosome 20 Syndrome | Semantic Scholar
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The evolving electroclinical syndrome of “epilepsy with ring chromosome 20” - ScienceDirect
John Libbey Eurotext - Epilepsies - Ring chromosome 20 and epilepsy: diversity of seizures presented by the patients as studied in video-EEG study. Is a subcortical dysfunctionning mainly involved in the epileptogenesis?
Ring Chromosomes - Ring20 Research and Support UK CIO
John Libbey Eurotext - Médecine thérapeutique / Pédiatrie - Apport de l'EEG dans le diagnostic et le suivi des épilepsies de l'enfant
Electroclinical evolution in ring chromosome 20 epilepsy syndrome: A case with severe phenotypic features followed for 25 years - ScienceDirect
Ring Chromosome 20 Neuropsychomotor Development - Candidate Genes
Crises d'épilepsie et mosaïque comportant un chromosome 20 en anneau
Épilepsie et chromosome
Electroclinical evolution in ring chromosome 20 epilepsy syndrome: A case with severe phenotypic features followed for 25 years - ScienceDirect
Molecular analysis of ring chromosome 20 syndrome reveals two distinct groups of patients | Journal of Medical Genetics
Chromosome 20 humain — Wikipédia
