21 results on '"Maillard, Camille"'
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2. Human neuropathology confirms projection neuron and interneuron defects and delayed oligodendrocyte production and maturation in FOXG1 syndrome
3. Mutations in TBR1 gene leads to cortical malformations and intellectual disability
4. TLE1, a key player in neurogenesis, a new candidate gene for autosomal recessive postnatal microcephaly
5. Tubulin mutations in human neurodevelopmental disorders
6. Delineating FOXG1 syndrome: From congenital microcephaly to hyperkinetic encephalopathy
7. Capturing the pathomechanisms of different disease severities in a human cerebral organoid model of LIS1-lissencephaly
8. Recurrent KIF2A mutations are responsible for classic lissencephaly
9. WDR81 mutations cause extreme microcephaly and impair mitotic progression in human fibroblasts and Drosophila neural stem cells
10. 2D and 3D Human Induced Pluripotent Stem Cell-Based Models to Dissect Primary Cilium Involvement during Neocortical Development
11. Neuropathological Hallmarks of Brain Malformations in Extreme Phenotypes Related to DYNC1H1 Mutations
12. Prenatal and Postnatal Presentations of Corpus Callosum Agenesis with Polymicrogyria Caused By EGP5 Mutation
13. A novel recurrent LIS1 splice site mutation in classic lissencephaly
14. Mutations in the Heterotopia Gene Eml1/EML1 Severely Disrupt the Formation of Primary Cilia
15. Recurrent RTTN mutation leading to severe microcephaly, polymicrogyria and growth restriction
16. Delineating FOXG1 syndrome
17. DelineatingFOXG1syndrome
18. A novel recurrent LIS1 splice site mutation in classic lissencephaly
19. Recurrent KIF2A mutations are responsible for classic lissencephaly
20. Mutations in the Heterotopia Gene Eml1/EML1Severely Disrupt the Formation of Primary Cilia
21. Tubulinopathies Overview
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