“…Gains at chromosomes 4, 6, 8, and X and losses on chromosomes 17, 22, and Y are the most frequent chromosomal abnormalities detected [11, 20–23]. Moreover, Schick [21] described the gene AURKA (20q13.2), a centrosome-associated serine/threonine kinase, with a possible role in chromosomal and genetic instability in JA.…”