IGF2, H19, CDKN1C and KCNQ1OT1 and the Beckwith-Wiedemann Syndrome

Marcel Mannens, I. Karen Temple, Frédéric Brioude

Research output: Chapter in Book/Report/Conference proceedingChapterAcademicpeer-review

Original languageEnglish
Title of host publicationEpstein’s inborn errors of development
Subtitle of host publicationThe molecular basis of clinical disorders of morphogenesis
EditorsRobert P. Erickson, Anthony J. Wynshaw-Boris
PublisherOxford University Press
Edition3th ed
ISBN (Print)9780199934522
Publication statusPublished - 2016

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