Table of Contents

Preface: Poot, M.; Genome Arrays for the Detection of Copy Number Variations in Idiopathic Mental Retardation, Idiopathic Generalized Epilepsy and Neuropsychiatric Disorders: Lessons for Diagnostic Workflow and Research: Hochstenbach, R.; Buizer-Voskamp, J.E.; Vorstman, J.A.S.; Ophoff, R.A.; Clinical Laboratory Implementation of Cytogenomic Microarrays: South, S.T.; Brothman, A.R.; SNP Array Analysis in Constitutional and Cancer Genome Diagnostics - Copy Number Variants, Genotyping and Quality Control: de Leeuw, N.; Hehir-Kwa, J.Y.; Simons, A.; Geurts van Kessel, A.; Smeets, D.F.; Faas, B.H.W.; Pfundt, R.; Interpretation of Array Comparative Genome Hybridization Data: A Major Challenge: Gijsbers, A.C.J.; Schoumans, J.; Ruivenkamp, C.A.L.; Disentangling the Myriad Genomics of Complex Disorders, Specifically Focusing on Autism, Epilepsy, and Schizophrenia: Poot, M.; van der Smagt, J.J.; Brilstra, E.H.; Bourgeron, T.; From Karyotyping to Array-CGH in Prenatal Diagnosis: Lichtenbelt, K.D.; Knoers, N.V.A.M.; Schuring-Blom, G.H.; Challenges of Interpreting Copy Number Variation in Syndromic and Non-Syndromic Congenital Heart Defects: Breckpot, J.; Thienpont, B.; Arens, Y.; Tranchevent, L.C.; Vermeesch, J.R.; Moreau, Y.; Gewillig, M.; Devriendt, K.; Array CGH in Human Leukemia: From Somatics to Genetics: van der Veken, L.T.; Buijs, A.; Origins and Breakpoint Analyses of Copy Number Variations: Up Close and Personal: van Binsbergen, E.; Functional Enrichment Analysis with Structural Variants: Pitfalls and Strategies: Webber, C.; Author Index.