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

Marcel Mannens; I. Karen Temple; Frédéric Brioude

doi:https://doi.org/10.1093/med/9780199934522.003.0143

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

Marcel Mannens, I. Karen Temple, Frédéric Brioude

Research output: Chapter in Book/Report/Conference proceeding › Chapter › Academic › peer-review

Original language	English
Title of host publication	Epstein’s inborn errors of development
Subtitle of host publication	The molecular basis of clinical disorders of morphogenesis
Editors	Robert P. Erickson, Anthony J. Wynshaw-Boris
Publisher	Oxford University Press
Pages	965-971
Edition	3th ed
ISBN (Print)	9780199934522
DOIs	https://doi.org/10.1093/med/9780199934522.003.0143
Publication status	Published - 2016

Access to Document

https://doi.org/10.1093/med/9780199934522.003.0143

Cite this

Mannens, M., Temple, I. K., & Brioude, F. (2016). IGF2, H19, CDKN1C and KCNQ1OT1 and the Beckwith-Wiedemann Syndrome. In R. P. Erickson, & A. J. Wynshaw-Boris (Eds.), Epstein’s inborn errors of development: The molecular basis of clinical disorders of morphogenesis (3th ed ed., pp. 965-971). Oxford University Press. https://doi.org/10.1093/med/9780199934522.003.0143

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IGF2, H19, CDKN1C and KCNQ1OT1 and the Beckwith-Wiedemann Syndrome. / Mannens, Marcel; Temple, I. Karen; Brioude, Frédéric.
Epstein’s inborn errors of development: The molecular basis of clinical disorders of morphogenesis. ed. / Robert P. Erickson; Anthony J. Wynshaw-Boris. 3th ed. ed. Oxford University Press, 2016. p. 965-971.

Research output: Chapter in Book/Report/Conference proceeding › Chapter › Academic › peer-review

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AU - Brioude, Frédéric

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BT - Epstein’s inborn errors of development

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