A statistical method for single sample analysis of HumanMethylation450 array data: genome-wide methylation analysis of patients with imprinting disorders.
about
Mutations in NLRP5 are associated with reproductive wastage and multilocus imprinting disorders in humans.Stochastic epigenetic mutations (DNA methylation) increase exponentially in human aging and correlate with X chromosome inactivation skewing in femalesNew developments in Silver-Russell syndrome and implications for clinical practiceDNA methylation analysis in constitutional disorders: Clinical implications of the epigenome.Diagnosis and management of Silver-Russell syndrome: first international consensus statement.
P2860
A statistical method for single sample analysis of HumanMethylation450 array data: genome-wide methylation analysis of patients with imprinting disorders.
description
2015 nî lūn-bûn
@nan
2015 թուականի Ապրիլին հրատարակուած գիտական յօդուած
@hyw
2015 թվականի ապրիլին հրատարակված գիտական հոդված
@hy
2015年の論文
@ja
2015年論文
@yue
2015年論文
@zh-hant
2015年論文
@zh-hk
2015年論文
@zh-mo
2015年論文
@zh-tw
2015年论文
@wuu
name
A statistical method for singl ...... nts with imprinting disorders.
@ast
A statistical method for singl ...... nts with imprinting disorders.
@en
type
label
A statistical method for singl ...... nts with imprinting disorders.
@ast
A statistical method for singl ...... nts with imprinting disorders.
@en
prefLabel
A statistical method for singl ...... nts with imprinting disorders.
@ast
A statistical method for singl ...... nts with imprinting disorders.
@en
P2093
P2860
P50
P1433
P1476
A statistical method for singl ...... ents with imprinting disorders
@en
P2093
Louise E Docherty
Rebecca L Poole
S Hasan Arshad
P2860
P2888
P356
10.1186/S13148-015-0081-5
P577
2015-04-21T00:00:00Z
P5875
P6179
1043287690