A genome-wide investigation of copy number variation in patients with sporadic brain arteriovenous malformation.
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Genome-wide association study of sporadic brain arteriovenous malformations.Molecular, Cellular, and Genetic Determinants of Sporadic Brain Arteriovenous Malformations.Genomic copy number variation analysis in multiple system atrophy.Identification of a rare BMP pathway mutation in a non-syndromic human brain arteriovenous malformation via exome sequencing.
P2860
A genome-wide investigation of copy number variation in patients with sporadic brain arteriovenous malformation.
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2013 nî lūn-bûn
@nan
2013 թուականի Հոկտեմբերին հրատարակուած գիտական յօդուած
@hyw
2013 թվականի հոտեմբերին հրատարակված գիտական հոդված
@hy
2013年の論文
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2013年論文
@yue
2013年論文
@zh-hant
2013年論文
@zh-hk
2013年論文
@zh-mo
2013年論文
@zh-tw
2013年论文
@wuu
name
A genome-wide investigation of ...... in arteriovenous malformation.
@ast
A genome-wide investigation of ...... in arteriovenous malformation.
@en
type
label
A genome-wide investigation of ...... in arteriovenous malformation.
@ast
A genome-wide investigation of ...... in arteriovenous malformation.
@en
prefLabel
A genome-wide investigation of ...... in arteriovenous malformation.
@ast
A genome-wide investigation of ...... in arteriovenous malformation.
@en
P2093
P2860
P50
P1433
P1476
A genome-wide investigation of ...... in arteriovenous malformation.
@en
P2093
Bobby P C Koeleman
Catharina J M Klijn
Charles E McCulloch
Diana E Guo
Jonathan G Zaroff
Ludmila Pawlikowska
Nasrine Bendjilali
Shantel Weinsheimer
Stephen Sidney
P2860
P304
P356
10.1371/JOURNAL.PONE.0071434
P407
P577
2013-10-03T00:00:00Z