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Abnormalities of the DNA methylation mark and its machinery: an emerging cause of neurologic dysfunctionMethylation analysis and diagnostics of Beckwith-Wiedemann syndrome in 1,000 subjects.The maternal to zygotic transition in mammals.Small regulatory RNAs controlled by genomic imprinting and their contribution to human disease.The epigenetic landscape of aneuploidy: constitutional mosaicism leading the way?Maternal fertility problems and risk for transient neonatal diabetes mellitus.Epimutation profiling in Beckwith-Wiedemann syndrome: relationship with assisted reproductive technology.Ensemble-Based Virtual Screening and Experimental Validation of Inhibitors Targeting a Novel Site of Human DNMT1.Establishing the clinical utility of epigenetic markers in cancer: many challenges ahead
P2860
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P2860
description
article científic
@ca
article scientifique
@fr
articol științific
@ro
articolo scientifico
@it
artigo científico
@gl
artigo científico
@pt
artigo científico
@pt-br
artikel ilmiah
@id
artikull shkencor
@sq
artículo científico
@es
name
Human imprinting syndromes.
@en
Human imprinting syndromes.
@nl
type
label
Human imprinting syndromes.
@en
Human imprinting syndromes.
@nl
prefLabel
Human imprinting syndromes.
@en
Human imprinting syndromes.
@nl
P2860
P356
P1433
P1476
Human imprinting syndromes
@en
P2093
Eamonn R Maher
P2860
P304
P356
10.2217/EPI.09.24
P50
P577
2009-12-01T00:00:00Z