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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 conference › Abstract › Other 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
Pages231
Number of pages1
Publication statusPublished - 21 Sept 2008
Event8th European Congress on Epileptology - Berlin
Duration: 21 Sept 2008 → 25 Sept 2008

Conference

Conference8th European Congress on Epileptology
CityBerlin
Period21/09/08 → 25/09/08

Keywords

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

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