about
TUBB2B Mutation in an Adult Patient with Myoclonus-Dystonia.Germline and somatic mutations in cortical malformations: Molecular defects in Argentinean patients with neuronal migration disorders.An in vitro model of lissencephaly: expanding the role of DCX during neurogenesis.KIAA1109 Variants Are Associated with a Severe Disorder of Brain Development and Arthrogryposis.Dysplasia and overgrowth: magnetic resonance imaging of pediatric brain abnormalities secondary to alterations in the mechanistic target of rapamycin pathway.Atypical Callosal Morphology in Children with Speech Sound Disorder.An Essential Postdevelopmental Role for Lis1 in Mice.Chromothripsis and ring chromosome 22: a paradigm of genomic complexity in the Phelan-McDermid syndrome (22q13 deletion syndrome).HCN2 Rescues brain defects by enforcing endogenous voltage pre-patterns.Homozygous null variant in CRADD, encoding an adaptor protein that mediates apoptosis, is associated with lissencephaly.The Case for Laboratory Developed Procedures: Quality and Positive Impact on Patient Care.
P2860
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P2860
description
2016 nî lūn-bûn
@nan
2016 թուականի Սեպտեմբերին հրատարակուած գիտական յօդուած
@hyw
2016 թվականի սեպտեմբերին հրատարակված գիտական հոդված
@hy
2016年の論文
@ja
2016年論文
@yue
2016年論文
@zh-hant
2016年論文
@zh-hk
2016年論文
@zh-mo
2016年論文
@zh-tw
2016年论文
@wuu
name
Genetic Basis of Brain Malformations
@ast
Genetic Basis of Brain Malformations
@en
Genetic Basis of Brain Malformations
@nl
type
label
Genetic Basis of Brain Malformations
@ast
Genetic Basis of Brain Malformations
@en
Genetic Basis of Brain Malformations
@nl
prefLabel
Genetic Basis of Brain Malformations
@ast
Genetic Basis of Brain Malformations
@en
Genetic Basis of Brain Malformations
@nl
P2860
P50
P356
P1476
Genetic Basis of Brain Malformations
@en
P2093
Renzo Guerrini
P2860
P304
P356
10.1159/000448639
P407
P577
2016-08-27T00:00:00Z