| Authors: |
Gaasterland CMW; Department of Clinical Epidemiology, Leiden University Medical Center, Leiden, The Netherlands; European Reference Network on Rare Congenital Malformations and Rare Intellectual Disability ERN-ITHACA, Clinical Genetics Department, Robert Debré University Hospital, Paris, France. Electronic address: c.m.w.gaasterland@lumc.nl., Klein Haneveld MJ; European Reference Network on Rare Congenital Malformations and Rare Intellectual Disability ERN-ITHACA, Clinical Genetics Department, Robert Debré University Hospital, Paris, France; Amsterdam UMC, Emma Children's Hospital, University of Amsterdam, Amsterdam, The Netherlands., Tinselboer BM; Advisium, 's Heeren Loo Zorggroep, Amersfoort, The Netherlands; European Foundation for SATB2-Associated Syndrome (SATB2 Europe)., Zarate YA; Division of Genetics and Metabolism, University of Kentucky, Lexington, KY, USA; Section of Genetics and Metabolism, University of Arkansas for Medical Sciences, Little Rock, AR, USA., Osredkar D; Department for Pediatric Neurology, University Children's Hospital Ljubljana, University Medical Centre Ljubljana, Ljubljana, Slovenia., van Eeghen AM; Amsterdam UMC, Emma Children's Hospital, University of Amsterdam, Amsterdam, The Netherlands; Advisium, 's Heeren Loo Zorggroep, Amersfoort, The Netherlands., Stariha E; European Reference Network on Rare Congenital Malformations and Rare Intellectual Disability ERN-ITHACA, Clinical Genetics Department, Robert Debré University Hospital, Paris, France; European Foundation for SATB2-Associated Syndrome (SATB2 Europe). |
