publication venue for
- Pre- and Postnatal Characterization of Autosomal Recessive <b><i>KIDINS220</i></b>-Associated Ventriculomegaly. 13:419-424. 2022
- Renpenning Syndrome in a Turkish Patient: de novo Variant c.607C>T in <b><i>PACS1</i></b> and Hypogammaglobulinemia Phenotype. 11:157-161. 2020
- Phenotypic Variability from Benign Infantile Epilepsy to Ohtahara Syndrome Associated with a Novel Mutation in SCN2A. 7:182-188. 2016