The KCNQ1OT1 imprinting control region and non-coding RNA: New properties derived from the study of Beckwith-Wiedemann syndrome and Silver-Russell syndrome cases

Human Molecular Genetics

Volumn 21, Issue 1, 2012, Pages 10-25

  Chiesa, Nicoletta ^a   De Crescenzo, Agostina ^b   Mishra, Kankadeb ^c   Perone, Lucia ^d   Carella, Massimo ^e   Palumbo, Orazio ^e   Mussa, Alessandro ^a   Sparago, Angela ^b,f   Cerrato, Flavia ^b   Russo, Silvia ^g   Lapi, Elisabetta ^h   Cubellis, Maria Vittoria ⁱ   Kanduri, Chandrasekhar ^c,j   Silengo, Margherita Cirillo ^a   Riccio, Andrea ^b,f   Ferrero, Giovanni Battista ^a  

^a UNIVERSITY OF TURIN   (Italy)

^b SECOND UNIVERSITY OF NAPLES   (Italy)

^c UPPSALA UNIVERSITY   (Sweden)

^d TELETHON INSTITUTE OF GENETICS AND MEDICINE TIGEM   (Italy)

^e CASA SOLLIEVO DELLA SOFFERENZA HOSPITAL   (Italy)

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

^g ISTITUTO AUXOLOGICO ITALIANO   (Italy)

^h UNIVERSITY OF FLORENCE   (Italy)

ⁱ UNIVERSITY OF NAPLES FEDERICO II   (Italy)

^j UNIVERSITY OF GOTHENBURG   (Sweden)

more..

Author keywords

[No Author keywords available]

Indexed keywords

POTASSIUM CHANNEL KCNQ1; UNTRANSLATED RNA;

ADULT; ARTICLE; BECKWITH WIEDEMANN SYNDROME; CASE REPORT; CELL CLONE; CENTROMERE; CHILD; CHROMATIN; CHROMOSOME 11P; CHROMOSOME MOSAICISM; DNA METHYLATION; FEMALE; GENE CLUSTER; GENE DUPLICATION; GENE EXPRESSION; GENE LOCUS; GENE SEQUENCE; GENE SILENCING; GENOME IMPRINTING; HUMAN; MALE; PHENOTYPE; PRESCHOOL CHILD; PRIORITY JOURNAL; PROTEIN DOMAIN; SEQUENCE ANALYSIS; SILVER RUSSELL SYNDROME;

ADULT; BECKWITH-WIEDEMANN SYNDROME; CHILD, PRESCHOOL; CHROMATIN; CHROMOSOMES, HUMAN, PAIR 11; DNA METHYLATION; FEMALE; GENE DUPLICATION; GENE SILENCING; GENOMIC IMPRINTING; HUMANS; INFANT; MALE; PEDIGREE; POTASSIUM CHANNELS, VOLTAGE-GATED; PROTEIN BINDING; RNA, UNTRANSLATED; SILVER-RUSSELL SYNDROME;

EID: 83455213564     PISSN: 09646906     EISSN: 14602083     Source Type: Journal    
DOI: 10.1093/hmg/ddr419     Document Type: Article

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