The KCNQ1OT1 imprinting control region and non-coding RNA: new properties derived from the study of Beckwith–Wiedemann syndrome and Silver–Russell syndrome cases-Reference-Cited by-同舟云学术

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

Published:2011-09-14 Issue:1 Volume:21 Page:10-25
ISSN:1460-2083
Container-title:Human Molecular Genetics
language:en
Short-container-title:

Author:

Chiesa Nicoletta,De Crescenzo Agostina,Mishra Kankadeb,Perone Lucia,Carella Massimo,Palumbo Orazio,Mussa Alessandro,Sparago Angela,Cerrato Flavia,Russo Silvia,Lapi Elisabetta,Cubellis Maria Vittoria,Kanduri Chandrasekhar,Cirillo Silengo Margherita,Riccio Andrea,Ferrero Giovanni Battista

Publisher

Oxford University Press (OUP)

Subject

Genetics (clinical),Genetics,Molecular Biology,General Medicine

Link

http://academic.oup.com/hmg/article-pdf/21/1/10/17254916/ddr419.pdf

Reference35 articles.

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4. Loss of imprinting of a paternally expressed transcript, with antisense orientation to KVLQT1, occurs frequently in Beckwith—Wiedemann syndrome and is independent of insulin-like growth factor II imprinting;Lee;Proc. Natl Acad. Sci. USA,1999

5. A maternally methylated CpG island in KvLQT1 is associated with an antisense paternal transcript and loss of imprinting in Beckwith—Wiedemann syndrome;Smilinich;Proc. Natl Acad. Sci. USA,1999

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