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Publication Reprint Request

Title: 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.
Authors: Lee MP,  DeBaun MR,  Mitsuya K,  Galonek HL,  Brandenburg S,  Oshimura M,  Feinberg AP
Journal: Proc Natl Acad Sci U S A 96(9):5203-8
Date: 1999 Apr 27
Branches: GEB
PubMedID: 10220444

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