Genome-wide DNA methylation analysis of patients with imprinting disorders identifies differentially methylated regions associated with novel candidate imprinted genes
about
Profound parental bias associated with chromosome 14 acquired uniparental disomy indicates targeting of an imprinted locusSNP-guided identification of monoallelic DNA-methylation events from enrichment-based sequencing data.A statistical method for single sample analysis of HumanMethylation450 array data: genome-wide methylation analysis of patients with imprinting disorders.Genome-wide DNA methylation analysis of transient neonatal diabetes type 1 patients with mutations in ZFP57Trisomy 21 Alters DNA Methylation in Parent-of-Origin-Dependent and -Independent Manners.Genome-Wide DNA Methylation Analysis and Epigenetic Variations Associated with Congenital Aortic Valve Stenosis (AVS).Mutations in NLRP5 are associated with reproductive wastage and multilocus imprinting disorders in humans.Genome-wide DNA methylation analysis of pseudohypoparathyroidism patients with GNAS imprinting defects.A multi-method approach to the molecular diagnosis of overt and borderline 11p15.5 defects underlying Silver-Russell and Beckwith-Wiedemann syndromesPervasive polymorphic imprinted methylation in the human placenta.DNA Methylation Profiling of Uniparental Disomy Subjects Provides a Map of Parental Epigenetic Bias in the Human GenomeEpigenetic markers for newborn congenital heart defect (CHD).DNA methylation analysis in constitutional disorders: Clinical implications of the epigenome.Diagnosis and management of Silver-Russell syndrome: first international consensus statement.An Update on Molecular Diagnostic Testing of Human Imprinting Disorders.Genome-wide analysis of differential DNA methylation in Silver-Russell syndrome.Analysis of Imprinted Gene Regulation.DNA Methylation Signatures of Early Childhood Malnutrition Associated With Impairments in Attention and Cognition.Expert consensus document: Clinical and molecular diagnosis, screening and management of Beckwith-Wiedemann syndrome: an international consensus statement.Mosaicism for trisomy 21: a review.Maternal 5mCpG Imprints at the PARD6G-AS1 and GCSAML Differentially Methylated Regions Are Decoupled From Parent-of-Origin Expression Effects in Multiple Human Tissues.Genome-Wide Association Study Identifies a Susceptibility Locus for Comitant Esotropia and Suggests a Parent-of-Origin EffectGenome-wide survey of parent-of-origin effects on DNA methylation identifies candidate imprinted loci in humansParent of origin gene expression in a founder population identifies two new candidate imprinted genes at known imprinted regions
P2860
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P2860
Genome-wide DNA methylation analysis of patients with imprinting disorders identifies differentially methylated regions associated with novel candidate imprinted genes
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2014 թուականի Ապրիլին հրատարակուած գիտական յօդուած
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2014 թվականի ապրիլին հրատարակված գիտական հոդված
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2014年の論文
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2014年論文
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2014年論文
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2014年論文
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2014年論文
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2014年論文
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2014年论文
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name
Genome-wide DNA methylation an ...... ovel candidate imprinted genes
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Genome-wide DNA methylation an ...... ovel candidate imprinted genes
@en
Genome-wide DNA methylation an ...... ovel candidate imprinted genes
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Genome-wide DNA methylation an ...... ovel candidate imprinted genes
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Genome-wide DNA methylation an ...... ovel candidate imprinted genes
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Genome-wide DNA methylation an ...... ovel candidate imprinted genes
@nl
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Genome-wide DNA methylation an ...... ovel candidate imprinted genes
@ast
Genome-wide DNA methylation an ...... ovel candidate imprinted genes
@en
Genome-wide DNA methylation an ...... ovel candidate imprinted genes
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P2093
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P50
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Genome-wide DNA methylation an ...... ovel candidate imprinted genes
@en
P2093
Hannah Jagoe
Hannah Lake
Hasan Arshad
Louise E Docherty
Rebecca L Poole
P2860
P304
P3181
P356
10.1136/JMEDGENET-2013-102116
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P50
P577
2014-02-05T00:00:00Z