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Tatton-Brown,                K, Loveday,                C, Yost,                S, Clarke,                M, Ramsay,                E,                Zachariou,              A, et al.            Childhood Overgrowth Collaboration. Mutations            in epigenetic regulation genens are a major cause of overgrowth with intellectual            disability. Am J Hum Genet          2017;100: 725\u201336.","DOI":"10.1016\/j.ajhg.2017.03.010"},{"key":"2","doi-asserted-by":"crossref","unstructured":"2. Ciolfi,              A,                Aref-Eshghi,              E, Pizzi,                S, Pedace,                L, Miele,                E, Kerkhof,                J, et al.            Frameshift mutations at the C-terminus of HIST1H1E result in a specific            DNA hypomethylation signature. Clin Epigenetics          2020;12: 7.","DOI":"10.1186\/s13148-019-0804-0"},{"key":"3","doi-asserted-by":"crossref","unstructured":"3. Takenouchi,                T, Uehara,                T, Kosaki,                K, Mizuno,                S. Growth            pattern of Rahman syndrome. Am J Med Genet A          2018;176: 712\u20134.","DOI":"10.1002\/ajmg.a.38616"},{"key":"4","doi-asserted-by":"crossref","unstructured":"4. Zhao,              J, Lyu,                G, Ding,                C, Wang,                X, Li,                J, Zhang,                W, et al.            Expanding the mutational spectrum of Rahman syndrome: A rare disorder            with severe intellectual disability and particular facial features in two Chinese            patients. Mol Genet Genomic Med          2022;10: e1825.","DOI":"10.1002\/mgg3.1825"},{"key":"5","doi-asserted-by":"crossref","unstructured":"5. Burkardt,                DD,                Zachariou,              A, Loveday,                C, Allen,                CL, Amor,                DJ,                Ardissone,              A, et al.              <i>HIST1H1E<\/i> heterozygous protein-truncating variants            cause a recognizable syndrome with intellectual disability and distinctive facial            gestalt: A study to clarify the HIST1H1E syndrome phenotype in 30            individuals. 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