Benign and Pathological Chromosomal Imbalances Microscopic and Submicroscopic Copy Number Variations (Cnvs) in Genetics and Counseling

"This volume systematically clarifies the disease implications of cytogenetically visible copy number variants (CG-CNV) using cytogenetic assessment of heterochromatic or euchromatic DNA variants.deep chromosome analysis and molecular cytogenetics remains relevant for technology translation, study design, and therapeutic assessment." --Anticancer Research 34, 2014

"Liehr.surveys the current knowledge of variation in the human genome, including the increasing number of alterations that seem to have no phenotypic consequences - a phenomenon once thought rare if not impossible. Focusing on cytogenetically visible copy number variants (CG-CNVs), he considers what the norm is, inheritance, formation, types, and their role on genetic diagnostics and counseling." --Reference & Research Book News, December 2013