Erratum: The 2q23.1 microdeletion syndrome: Clinical and behavioural phenotype (European Journal of Human Genetics (2010) 18 (163-170) DOI: 10.1038/ejhg.2009.152)

Bregje W M Van Bon, David A. Koolen, Louise Brueton, Dominic McMullan, Klaske D. Lichtenbelt, Lesley C. Adès, Gregory Peters, Kate Gibson, Susan Moloney, Francesca Novara, Tiziano Pramparo, Bernardo Dalla Bernardina, Leonardo Zoccante, Umberto Balottin, Fausta Piazza, Vanna Pecile, Paolo Gasparini, Veronica Guerci, Marleen Kets, Rolph PfundtArjan P. De Brouwer, Joris A. Veltman, Nicole De Leeuw, Meredith Wilson, Jayne Antony, Santina Reitano, Daniela Luciano, Marco Fichera, Corrado Romano, Han G. Brunner, Orsetta Zuffardi, Bert B A De Vries

Research output: Contribution to journalArticlepeer-review

Original languageEnglish
Pages (from-to)1171
Number of pages1
JournalEuropean Journal of Human Genetics
Volume18
Issue number10
DOIs
Publication statusPublished - Oct 2010

ASJC Scopus subject areas

  • Genetics(clinical)
  • Genetics

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