Pages that link to "Q36142055"
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The following pages link to Genotype-phenotype correlation in lissencephaly and subcortical band heterotopia: the key questions answered (Q36142055):
Displaying 12 items.
- Mutations in alpha-tubulin cause abnormal neuronal migration in mice and lissencephaly in humans (Q34600929) (← links)
- Lissencephaly and mild cerebellar vermis hypoplasia in a case of microcephaly and chorioretinal dysplasia (Q41936762) (← links)
- Tubulinopathies and Their Brain Malformation Syndromes: Every TUB on Its Own Bottom (Q42405349) (← links)
- Pattern of childhood epilepsies with neuronal migrational disorders in Oman (Q45863711) (← links)
- Lissencephaly type I. (Q46353154) (← links)
- Lissencephaly and band heterotopia: LIS1, TUBA1A, and DCX mutations in Hungary (Q48619542) (← links)
- Subcortical laminar (band) heterotopia (Q48914651) (← links)
- Voxel-based 3D MRI analysis helps to detect subtle forms of subcortical band heterotopia. (Q51899488) (← links)
- A novel missense mutation in LIS1 in a child with subcortical band heterotopia and pachygyria inherited from his mildly affected mother with somatic mosaicism (Q51924992) (← links)
- Neuropsychological profile of children with subcortical band heterotopia (Q51956870) (← links)
- Novel DCX mutation-caused lissencephaly in a boy and very mild heterotopia in his mother. (Q53546732) (← links)
- Spontaneous epileptiform activity in a rat model of bilateral subcortical band heterotopia (Q63433200) (← links)