The clinical benefit of array-based comparative genomic hybridization for detection of copy number variants in Czech children with intellectual disability and developmental delay

• Main Authors: Marketa Wayhelova (Author), Jan Smetana (Author), Vladimira Vallova (Author), Eva Hladilkova (Author), Hana Filkova (Author), Marta Hanakova (Author), Marcela Vilemova (Author), Petra Nikolova (Author), Barbora Gromesova (Author), Renata Gaillyova (Author), Petr Kuglik (Author)
• Format: Book
• Published: BMC, 2019-07-01T00:00:00Z.
• Subjects: article
• Online Access: Connect to this object online.

Abstract Background Chromosomal microarray analysis has been shown to be a valuable and cost effective assay for elucidating copy number variants (CNVs) in children with intellectual disability and developmental delay (ID/DD). Methods In our study, we performed array-based comparative genomic hybrid...