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Home > Our Research Activities > List Of Publications > Structural brain anomalies in Cri-du-Chat syndrome: MRI findings in 14 patients and possible genotype-phenotype correlations.

Structural brain anomalies in Cri-du-Chat syndrome: MRI findings in 14 patients and possible genotype-phenotype correlations.

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Large-scale targeted sequencing identifies risk genes for neurodevelopmental disorders.

ATP1A2- and ATP1A3- associated early profound epileptic encephalopathy and polymicrogyria.

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