Disruption of genomic neighbourhood at the imprinted IGF2-H19 locus in Beckwith-Wiedemann syndrome and Silver-Russell syndrome

Human Molecular Genetics

Volumn 20, Issue 7, 2011, Pages 1363-1374

  Nativio, Raffaella ^a   Sparago, Angela ^b   Ito, Yoko ^a   Weksberg, Rosanna ^c   Riccio, Andrea ^b,d   Murrell, Adele ^a  

^a UNIVERSITY OF CAMBRIDGE   (United Kingdom)

^b INSTITUTE OF GENETICS AND BIOPHYSICS ADRIANO BUZZATI TRAVERSO   (Italy)

^c HOSPITAL FOR SICK CHILDREN RESEARCH INSTITUTE   (Canada)

^d SECOND UNIVERSITY OF NAPLES   (Italy)

Author keywords

[No Author keywords available]

Indexed keywords

COHESIN; HISTONE H3; HISTONE H4; SOMATOMEDIN B; TRANSCRIPTION FACTOR CTCF;

ARTICLE; BECKWITH WIEDEMANN SYNDROME; BINDING SITE; CHROMATIN STRUCTURE; CONFORMATION; CONTROLLED STUDY; DNA FLANKING REGION; DNA METHYLATION; EPIGENETICS; GENE DISRUPTION; GENE LOCUS; GENETIC MARKER; HISTONE MODIFICATION; HUMAN; HUMAN CELL; LYMPHOBLASTOID CELL; PRIORITY JOURNAL; PROTEIN BINDING; PROTEIN PROTEIN INTERACTION; SILVER RUSSELL SYNDROME;

BECKWITH-WIEDEMANN SYNDROME; CELL CYCLE PROTEINS; CELL LINE, TUMOR; CHROMATIN; CHROMOSOMAL PROTEINS, NON-HISTONE; FEMALE; GENETIC LOCI; GENOMIC IMPRINTING; HISTONES; HUMANS; INSULIN-LIKE GROWTH FACTOR II; MALE; PROTEIN PROCESSING, POST-TRANSLATIONAL; REPRESSOR PROTEINS; SILVER-RUSSELL SYNDROME;

EID: 79952605614     PISSN: 09646906     EISSN: 14602083     Source Type: Journal    
DOI: 10.1093/hmg/ddr018     Document Type: Article

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