Genome architecture and its roles in human copy number variation.
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Major influence of repetitive elements on disease-associated copy number variants (CNVs)Genome annotation for clinical genomic diagnostics: strengths and weaknessesClinical implications of copy number variations in autoimmune disordersThe role of human endogenous retroviruses in brain development and function.De novo HNF1 homeobox B mutation as a cause for chronic, treatment-resistant hypomagnesaemia.
P2860
Genome architecture and its roles in human copy number variation.
description
2014 nî lūn-bûn
@nan
2014 թուականի Դեկտեմբերին հրատարակուած գիտական յօդուած
@hyw
2014 թվականի դեկտեմբերին հրատարակված գիտական հոդված
@hy
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
name
Genome architecture and its roles in human copy number variation.
@ast
Genome architecture and its roles in human copy number variation.
@en
type
label
Genome architecture and its roles in human copy number variation.
@ast
Genome architecture and its roles in human copy number variation.
@en
prefLabel
Genome architecture and its roles in human copy number variation.
@ast
Genome architecture and its roles in human copy number variation.
@en
P2093
P2860
P356
P1476
Genome architecture and its roles in human copy number variation
@en
P2093
P2860
P304
P356
10.5808/GI.2014.12.4.136
P50
P577
2014-12-31T00:00:00Z