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MOESM2 of A genome-wide DNA methylation signature for SETD1B-related syndrome

  • Izabela Krzyzewska (Contributor)
  • Saskia Maas (Contributor)
  • Peter Henneman (Contributor)
  • K. V. D. Lip (Contributor)
  • A. Venema (Amsterdam UMC) (Contributor)
  • K. Baranano (Contributor)
  • A. Chassevent (Contributor)
  • E. Aref-Eshghi (Contributor)
  • T. Fukuda (Contributor)
  • H. Ikeda (Contributor)
  • M. Jacquemont (Contributor)
  • H. G. Kim (Contributor)
  • A. Labalme (Contributor)
  • S. M. E. Lewis (Contributor)
  • G. Lesca (Contributor)
  • I. Madrigal (Contributor)
  • S. Mahida (Contributor)
  • N. Matsumoto (Contributor)
  • R. Rabionet (Contributor)
  • E. Rajcan-Separovic (Contributor)
  • Y. Qiao (Contributor)
  • B. Sadikovic (Contributor)
  • H. Saitsu (Contributor)
  • D. A. Sweetser (Contributor)
  • Mariëlle Alders (Contributor)
  • M.M.A.M. Mannens (University of Amsterdam) (Contributor)

Dataset

Description

Additional file 2: Table S2. Significant differentially methylated CpGs identified in the SETD1B-related group analysis.
Date made available2019
PublisherFigshare

Access Dataset

  • A genome-wide DNA methylation signature for SETD1B-related syndrome

    Krzyzewska, I. M., Maas, S. M., Henneman, P., Lip, K. V. D., Venema, A., Baranano, K., Chassevent, A., Aref-Eshghi, E., van Essen, A. J., Fukuda, T., Ikeda, H., Jacquemont, M., Kim, H. G., Labalme, A., Lewis, S. M. E., Lesca, G., Madrigal, I., Mahida, S., Matsumoto, N. & Rabionet, R. & 7 others, Rajcan-Separovic, E., Qiao, Y., Sadikovic, B., Saitsu, H., Sweetser, D. A., Alders, M. & Mannens, M. M. A. M., 2019, In: Clinical epigenetics. 11, 1, p. 156

    Research output: Contribution to journal › Article › Academic › peer-review

    Open Access
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