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    Koolen D A, Sharp A J, Hurst J A, Firth H V, Knight S J L et al. J Med Genet 2008;45:710–720. Dr Samantha Knight requested to revise some of her personal details. Her affiliation should be: Oxford Genetics Knowledge Park and NIHR Biomedical Research Centre, Oxford, The Wellcome Trust Centre for Human Genetics, Churchill Hospital, Oxford, UK.

    Acknowledgement: We would also like to acknowledge Dr Regina Regan (Oxford Genetics Knowledge Park and NIHR NIHR Biomedical Research Centre, Oxford) and Mrs Cheryl Guiver (Oxford Genetics Knowledge Park), and Cindy Skinner for their assistance.

    Funding: SJLK and RR were supported by the NIHR Biomedical Research Centre, Oxford and by the Oxford Genetics Knowledge Park.

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      Clinical and molecular delineation of the 17q21.31 microdeletion syndrome
      D A Koolen A J Sharp J A Hurst H V Firth S J L Knight A Goldenberg P Saugier-Veber R Pfundt L E L M Vissers A Destrée B Grisart L Rooms N Van der Aa M Field A Hackett K Bell M J M Nowaczyk G M S Mancini P J Poddighe C E Schwartz E Rossi M De Gregori L L Antonacci-Fulton M D McLellan II J M Garrett M A Wiechert T L Miner S Crosby R Ciccone L Willatt A Rauch M Zenker S Aradhya M A Manning T M Strom J Wagenstaller A C Krepischi-Santos A M Vianna-Morgante C Rosenberg S M Price H Stewart C Shaw-Smith H G Brunner A O M Wilkie J A Veltman O Zuffardi E E Eichler B B A de Vries
      Journal of Medical Genetics 2008; 45 710-720 Published Online First: 15 Jul 2008. doi: 10.1136/jmg.2008.058701