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syndrome lissencephaly
Summary
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Most Correlated Studies
OMIM - Congenital disorder
OMIM - Multisystem Complex Disorders
OMIM - Disorder of brain
Mouse Phenotypes - Lissencephaly
OMIM - Brain CNS Motor Neuron and other Neuropathy Disorders
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TUBA1A mutation-associated lissencephaly: case report and review of the literature.
Prenatal diagnosis of ring chromosome 2 with lissencephaly and 2p25.3 and 2q37.3 microdeletions dete…
Cobblestone lissencephaly: neuropathological subtypes and correlations with genes of dystroglycanopa…
Identification of mutations in TMEM5 and ISPD as a cause of severe cobblestone lissencephaly.
Post-natal treatment by a blood-brain-barrier permeable calpain inhibitor, SNJ1945 rescued defective…
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Investigation of the Usability of the Dynamic Scaffolding System
Clinical-genetic Investigations in Children With Early Infantile Epilepsies
Human Epilepsy Genetics--Neuronal Migration Disorders Study
Pilot Study of Rapid Whole Genome Sequencing of Severely Ill Patients in Pediatric Intensive Care in…
Prenatal Treatment of Congenital Cytomegalovirus Infection With Letermovir Versus Valaciclovir
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