Clinical Validation of a Genome-Wide DNA Methylation Assay for Molecular Diagnosis of Imprinting Disorders - Aref-Eshghi, Erfan; Schenkel, Laila C.; Lin, Hanxin; Skinner, Cindy; Ainsworth, Peter; Paré, Guillaume; Siu, Victoria; Rodenhiser, David; Schwartz, Charles; Sadikovic, Bekim (The Journal of molecular diagnostics : JMD, 2017)
Keywords: Angelman Syndrome - genetics; Angelman Syndrome - pathology; Beckwith-Wiedemann Syndrome - genetics; Beckwith-Wiedemann Syndrome - pathology; DNA Methylation - genetics; Epigenomics; Female; Gene Expression Regulation; Genome, Human; Genomic Imprinting - genetics; Humans; Male; Oligonucleotide Array Sequence Analysis - methods; Prader-Willi Syndrome - genetics; Prader-Willi Syndrome - pathology; Silver-Russell Syndrome - genetics; Silver-Russell Syndrome - pathology