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

Research output: Contribution to conferenceAbstractOther 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
Pages213
Number of pages1
Publication statusPublished - 2009
Event8th European Congress on Epileptology, Berlin -
Duration: 1 Jan 2009 → …

Conference

Conference8th European Congress on Epileptology, Berlin
Period1/01/09 → …

Keywords

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

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