Whole exome sequencing to find de novo causal variants: sample size and significance

Translated title of the contribution: Whole exome sequencing to find de novo causal variants: sample size and significance

C.G.F. de Kovel, B.P.C. Koeleman

Research output: Contribution to conferencePosterOther research output

Translated title of the contributionWhole exome sequencing to find de novo causal variants: sample size and significance
Original languageUndefined/Unknown
Publication statusPublished - 8 Jun 2013
EventEuropean Society for Human Genetics (ESHG) - Parijs, Frankrijk
Duration: 8 Jun 201311 Jun 2013

Conference

ConferenceEuropean Society for Human Genetics (ESHG)
CityParijs, Frankrijk
Period8/06/1311/06/13

Keywords

  • Econometric and Statistical Methods: General
  • Geneeskunde (GENK)
  • Geneeskunde(GENK)
  • Medical sciences
  • Bescherming en bevordering van de menselijke gezondheid

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