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polymicrogyria
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ADGRG1
SRPX2
RTTN
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angiogenesis
GUENTHER_GROWTH_SPHERICAL_VS_ADHERENT_UP
BYSTRYKH_HEMATOPOIESIS_STEM_CELL_QTL_CIS
GSE14415_NATURAL_TREG_VS_FOXP3_KO_NATURAL_TREG_DN
GSE32901_TH1_VS_TH17_NEG_CD4_TCELL_UP
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OMIM - Disorder of brain
OMIM - Congenital disorder
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Exome Sequencing and the Identification of New Genes and Shared Mechanisms in Polymicrogyria.
Polymicrogyria: An Unusual Case of Secondary Mania.
Hemidystonia with polymicrogyria is part of ATP1A3-related disorders.
Diverse genetic causes of polymicrogyria with epilepsy.
Polymicrogyria in a child with KCNMA1-related channelopathy.
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Assessment of the Efficacy and Safety of Alpelisib (BYL719) in Pediatric and Adult Patients With Meg…
Brain Development Research Program
Use of a Tonometer to Identify Epileptogenic Lesions During Pediatric Epilepsy Surgery
Epilepsy Phenome/Genome Project
Human Epilepsy Genetics--Neuronal Migration Disorders Study
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