about
Genome-wide association studies in neurological disordersCopy number variations and strokeAn integrated database-pipeline system for studying single nucleotide polymorphisms and diseases.Molecular cytogenetics and cytogenomics of brain diseases.Copy number variants in genetic susceptibility and severity of systemic lupus erythematosusRecurrent chromosome 16p13.1 duplications are a risk factor for aortic dissections.Assessment of copy number variation using the Illumina Infinium 1M SNP-array: a comparison of methodological approaches in the Spanish Bladder Cancer/EPICURO study.Development and application of genotyping technologies.The genetics of ischaemic stroke.Genetic Imbalance in Patients with Cervical Artery DissectionGenetics of ischaemic stroke.Genome-wide assessment of Parkinson's disease in a Southern Spanish population.
P2860
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P2860
description
2008 nî lūn-bûn
@nan
2008 թուականի Փետրուարին հրատարակուած գիտական յօդուած
@hyw
2008 թվականի փետրվարին հրատարակված գիտական հոդված
@hy
2008年の論文
@ja
2008年論文
@yue
2008年論文
@zh-hant
2008年論文
@zh-hk
2008年論文
@zh-mo
2008年論文
@zh-tw
2008年论文
@wuu
name
Structural genomic variation in ischemic stroke.
@ast
Structural genomic variation in ischemic stroke.
@en
type
label
Structural genomic variation in ischemic stroke.
@ast
Structural genomic variation in ischemic stroke.
@en
prefLabel
Structural genomic variation in ischemic stroke.
@ast
Structural genomic variation in ischemic stroke.
@en
P2093
P2860
P50
P1433
P1476
Structural genomic variation in ischemic stroke.
@en
P2093
Angela Britton
Bradford B Worrall
Dena G Hernandez
Hon-Chung Fung
J Raphael Gibbs
James F Meschia
Javier Simon-Sanchez
L Douglas Case
Mar Matarin
Robert D Brown
P2860
P2888
P304
P356
10.1007/S10048-008-0119-3
P50
P577
2008-02-21T00:00:00Z