Eight TFs and four ERFs are among the differentially expressed genes, as well as eight genes associated with Turner syndrome (PROCR, NR3C1, INSR, APOB, BMP15, F8, IL6, and WAS) [86–88] and two genes that are haploinsufficient in humans (RAD50 and SLC33A1) [88]. The gene discussed is HBS1L; the disease is Turner syndrome.