about
Advancing epilepsy genetics in the genomic eraGenetic Counseling for Autism Spectrum Disorder in an Evolving Theoretical LandscapeAnalysis of rare copy number variation in absence epilepsies.Identifying CNVs in 15q11q13 and 16p11.2 of Patients with Seizures Increases the Rates of Detecting Pathogenic Changes.Chromosomal Microarrays: Understanding Genetics of Neurodevelopmental Disorders and Congenital Anomalies.Identification of novel candidate disease genes from de novo exonic copy number variants.Association of Tag SNPs and Rare CNVs of the MIR155HG/miR-155 Gene with Epilepsy in the Chinese Han Population.Mapping a shared genetic basis for neurodevelopmental disorders.Prevalence of Pathogenic Copy Number Variation in Adults With Pediatric-Onset Epilepsy and Intellectual Disability.Next Generation Sequencing Methods for Diagnosis of Epilepsy Syndromes.
P2860
Q26798035-B54D3142-D7C2-4589-AE2C-63A389AEA47CQ28076465-2B5D2A91-FF42-4C04-9108-B6020E1D5D92Q36794058-21F6A362-B83B-41DD-B37A-124A57B4DA24Q37460174-69A053B4-BFDF-4FC5-8601-328FC0058E84Q39127499-2758EB95-5DF9-4B5D-8A27-77D93CD5138CQ41692239-D3656309-BC8B-48FE-A7CE-80FD036A22F0Q42179622-6362B6FF-872B-4C3F-A8A5-A4834A28E1CCQ47111463-B72A4C6F-33F9-407C-8F12-507B88279388Q47635812-7BF6A1F9-AECB-49F9-AE69-1F86E385C353Q52375104-75DA54E0-6465-412B-B225-7E1195EA4FF2
P2860
description
2014 nî lūn-bûn
@nan
2014年の論文
@ja
2014年論文
@yue
2014年論文
@zh-hant
2014年論文
@zh-hk
2014年論文
@zh-mo
2014年論文
@zh-tw
2014年论文
@wuu
2014年论文
@zh
2014年论文
@zh-cn
name
CNVs in Epilepsy.
@en
CNVs in Epilepsy.
@nl
type
label
CNVs in Epilepsy.
@en
CNVs in Epilepsy.
@nl
prefLabel
CNVs in Epilepsy.
@en
CNVs in Epilepsy.
@nl
P2860
P1476
CNVs in Epilepsy.
@en
P2093
Heather C Mefford
P2860
P2888
P304
P356
10.1007/S40142-014-0046-6
P577
2014-06-28T00:00:00Z
P5875
P6179
1016907782