• <em>DCX</em> variants in two unrelated Chinese families with subcortical band heterotopia: Two case reports and review of literature
• <em>PAFAH1B1</em>-Related Lissencephaly / Subcortical Band Heterotopia
• Analysis of ARX gene variant in a child with X-linked lissencephaly with abnormal genitalia
• Bi-allelic CAMSAP1 variants cause a clinically recognizable neuronal migration disorder
• Bi-allelic Loss of Human APC2, Encoding Adenomatous Polyposis Coli Protein 2, Leads to Lissencephaly, Subcortical Heterotopia, and Global Developmental Delay
• Bi-allelic Pathogenic Variants in TUBGCP2 Cause Microcephaly and Lissencephaly Spectrum Disorders
• Case Report: PAFAH1B1 Mutation and Posterior Band Heterotopia With Focal Temporal Lobe Epilepsy Treated by Responsive Neurostimulation
• DCX variants in two unrelated Chinese families with subcortical band heterotopia: Two case reports and review of literature
• Double cortex syndrome (subcortical band heterotopia): A case report
• Familial posterior predominant subcortical band heterotopia caused by a CEP85L missense mutation
• Further characterization of CEP85L-associated lissencephaly type 10: Report of a three-generation family and review of the literature
• Gastric heterotopia in the rectum: a rare entity with potential pitfalls
• Insights on the Role of α- and β-Tubulin Isotypes in Early Brain Development
• Neuronal migration genes and a familial translocation t (3;17): candidate genes implicated in the phenotype
• Novel COL4A2 mutation causing familial malformations of cortical development
• Novel lissencephaly-associated DCX variants in the C-terminal DCX domain affect microtubule binding and dynamics
• Novel role of the synaptic scaffold protein Dlgap4 in ventricular surface integrity and neuronal migration during cortical development
• PAFAH1B1-Related Lissencephaly / Subcortical Band Heterotopia
• Pathogenic Variants in CEP85L Cause Sporadic and Familial Posterior Predominant Lissencephaly
• Phenotypic Variability in Novel Doublecortin Gene Variants Associated with Subcortical Band Heterotopia
• Submicroscopic 11p13 deletion including the elongator acetyltransferase complex subunit 4 gene in a girl with language failure, intellectual disability and congenital malformations: A case report
• The clinical, imaging, pathological and genetic landscape of bottom-of-sulcus dysplasia