Interstitial deletions of chromosome 20: a common cause of benign familial neonatal convulsions as detected by MLPA and high resolution SNP array

Translated title of the contribution: Interstitial deletions of chromosome 20: a common cause of benign familial neonatal convulsions as detected by MLPA and high resolution SNP array

N.E. Verbeek, M.E.M. Swinkels, W. Arts, W. Gunning, P. Callenbach, M. Poot, D. Lindhout, M.J.A. van Kempen

Research output: Contribution to conferencePosterOther research output

Translated title of the contributionInterstitial deletions of chromosome 20: a common cause of benign familial neonatal convulsions as detected by MLPA and high resolution SNP array
Original languageUndefined/Unknown
Publication statusPublished - 21 Sept 2008
Event8th European Congress on Epileptology - Berlin
Duration: 21 Sept 200825 Sept 2008

Conference

Conference8th European Congress on Epileptology
CityBerlin
Period21/09/0825/09/08

Keywords

  • Econometric and Statistical Methods: General
  • Geneeskunde(GENK)

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