Gain of imprinting at chromosome 11p15: A pathogenetic mechanism identified in human hepatocarcinomas-Reference-Cited by-同舟云学术

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Gain of imprinting at chromosome 11p15: A pathogenetic mechanism identified in human hepatocarcinomas

Published:2000-04-25 Issue:10 Volume:97 Page:5445-5449
ISSN:0027-8424
Container-title:Proceedings of the National Academy of Sciences
language:en
Short-container-title:Proceedings of the National Academy of Sciences

Author:

Schwienbacher C.,Gramantieri L.,Scelfo R.,Veronese A.,Calin G. A.,Bolondi L.,Croce C. M.,Barbanti-Brodano G.,Negrini M.

Publisher

Proceedings of the National Academy of Sciences

Subject

Multidisciplinary

Reference38 articles.

1. Deletions of a differentially methylated CpG island at the SNRPN gene define a putative imprinting control region

2. Inherited microdeletions in the Angelman and Prader–Willi syndromes define an imprinting centre on human chromosome 15

3. Imprinting in clusters: lessons from Beckwith-Wiedemann syndrome

4. Beckwith-wiedemann syndrome, tumourigenesis and imprinting

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