Microdeletions in the human H19 DMR result in loss of IGF2 imprinting and Beckwith-Wiedemann syndrome.
Sparago A; Cerrato F; Vernucci M; Ferrero GB; Silengo MC; Riccio A; Nature Genetics, 2004, vol. 36, issue 9, p 958, ISSN 10614036. ISBN 10614036.

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