Pages that link to "Q28200024"
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The following pages link to Mutation analysis of the DCX gene and genotype/phenotype correlation in subcortical band heterotopia (Q28200024):
Displaying 50 items.
- Genetic Basis of Brain Malformations (Q28076998) (← links)
- (Q28158122) (redirect page) (← links)
- Mutation of the doublecortin gene in male patients with double cortex syndrome: somatic mosaicism detected by hair root analysis (Q28198469) (← links)
- Genetic malformations of the cerebral cortex and epilepsy (Q28243987) (← links)
- Dab2ip regulates neuronal migration and neurite outgrowth in the developing neocortex (Q28505693) (← links)
- Doublecortin recognizes the 13-protofilament microtubule cooperatively and tracks microtubule ends (Q29394565) (← links)
- Novel embryonic neuronal migration and proliferation defects in Dcx mutant mice are exacerbated by Lis1 reduction (Q30494259) (← links)
- Neuronal migration, cerebral cortical development, and cerebral cortical anomalies (Q30671553) (← links)
- Brain development and the genetics of brain development (Q30773677) (← links)
- The genetics of lissencephaly (Q30826834) (← links)
- Neuronal migration disorders, genetics, and epileptogenesis (Q30990797) (← links)
- Novel mental retardation-epilepsy syndrome linked to Xp21.1-p11.4. (Q34108701) (← links)
- Intragenic deletions and duplications of the LIS1 and DCX genes: a major disease-causing mechanism in lissencephaly and subcortical band heterotopia (Q34326750) (← links)
- Epilepsy and genetic malformations of the cerebral cortex (Q34386806) (← links)
- Role of cytoskeletal abnormalities in the neuropathology and pathophysiology of type I lissencephaly (Q34566623) (← links)
- Life is a journey: a genetic look at neocortical development (Q34623765) (← links)
- Brain malformations, epilepsy, and infantile spasms (Q34663411) (← links)
- Genetic malformations of the human frontal lobe (Q34743385) (← links)
- Malformations of cortical development: clinical features and genetic causes (Q35188898) (← links)
- Epilepsy as a neurodevelopmental disorder (Q35838099) (← links)
- The classification of cortical dysplasias through molecular genetics (Q35846477) (← links)
- Are Ectopic Neurons a Red Herring in Localizing Seizure Foci? (Q35923061) (← links)
- Genotype-phenotype correlation in lissencephaly and subcortical band heterotopia: the key questions answered (Q36142055) (← links)
- Lis1 and doublecortin function with dynein to mediate coupling of the nucleus to the centrosome in neuronal migration (Q36322452) (← links)
- New insights into genotype-phenotype correlations for the doublecortin-related lissencephaly spectrum (Q36581137) (← links)
- Cortical dysplasia: a possible substrate for brain tumors (Q36678551) (← links)
- Dcx reexpression reduces subcortical band heterotopia and seizure threshold in an animal model of neuronal migration disorder (Q37275380) (← links)
- A novel missense mutation of doublecortin: mutation analysis of Korean patients with subcortical band heterotopia (Q37433762) (← links)
- Genetic basis in epilepsies caused by malformations of cortical development and in those with structurally normal brain (Q37523411) (← links)
- SDF1 reduces interneuron leading process branching through dual regulation of actin and microtubules (Q37679317) (← links)
- Developments in Molecular Genetic Diagnostics: An Update for the Pediatric Epilepsy Specialist (Q37863822) (← links)
- Causes and consequences of gray matter heterotopia (Q38245494) (← links)
- Germline and somatic mutations in cortical malformations: Molecular defects in Argentinean patients with neuronal migration disorders. (Q42365189) (← links)
- The location of DCX mutations predicts malformation severity in X-linked lissencephaly (Q43502667) (← links)
- Lissencephaly type I. (Q46353154) (← links)
- Mitotic impairment by doublecortin is diminished by doublecortin mutations found in patients (Q47877140) (← links)
- Mosaic mutations of the LIS1 gene cause subcortical band heterotopia (Q48160883) (← links)
- Array-CGH in unclear syndromic nephropathies identifies a microdeletion in Xq22.3-q23. (Q48614777) (← links)
- Lissencephaly and band heterotopia: LIS1, TUBA1A, and DCX mutations in Hungary (Q48619542) (← links)
- Normotopic cortex is the major contributor to epilepsy in experimental double cortex. (Q48629894) (← links)
- Case report: Neuronal migration disorder associated with chromosome 15q13.3 duplication in a boy with autism and seizures. (Q48842137) (← links)
- Subcortical laminar (band) heterotopia (Q48914651) (← links)
- Subcortical band heterotopia with simplified gyral pattern and syndactyly (Q51948727) (← links)
- Educational, cognitive, behavioral and language development issues (Q51948887) (← links)
- Neuropsychological profile of children with subcortical band heterotopia (Q51956870) (← links)
- Lissencephaly: Expanded imaging and clinical classification. (Q52097470) (← links)
- Novel DCX mutation-caused lissencephaly in a boy and very mild heterotopia in his mother. (Q53546732) (← links)
- Malformations of cortical development and epilepsy (Q56232687) (← links)
- Mosaic DCX deletion causes subcortical band heterotopia in males (Q57199732) (← links)
- Comprehensive genotype-phenotype correlation in lissencephaly (Q58804647) (← links)