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Johnston,                JJ,                Olivos-Glander,              I, Killoran,                C, Elson,                E, Turner,                JT, Peters,                KF, et al.            Molecular and clinical analyses of Greig cephalopolysyndactyly and            Pallister-Hall syndromes: robust phenotype prediction from the type and position of              <i>GLI3<\/i> mutations. Am J Hum Genet          2005;76: 609\u201322.","DOI":"10.1086\/429346"},{"key":"2","doi-asserted-by":"crossref","unstructured":"2. Narumi,              Y, Kosho,                T, Tsuruta,                G,              Shiohara, M,                Shimazaki,              E, Mori,                T, et al.            Genital abnormalities in Pallister-Hall syndrome: Report of two patients            and review of the literature. Am J Med Genet A          2010;152A: 3143\u20137.","DOI":"10.1002\/ajmg.a.33720"},{"key":"3","doi-asserted-by":"crossref","unstructured":"3. Kiuchi,              K, Sato,                T, Nakano,                S, Ishii,                T,              Hasegawa,            T. Continuous            glucose monitoring in an infant with panhypopituitarism having hypoglycemia on growth            hormone therapy. J Pediatr Endocrinol Metab          2022;35: 1556\u20139.","DOI":"10.1515\/jpem-2022-0224"},{"key":"4","doi-asserted-by":"crossref","unstructured":"4. D\u00e9murger,                F, Ichkou,                A,                Mougou-Zerelli,              S, Le Merrer,                M,                Goudefroye,              G, Delezoide,                AL, et al.            New insights into genotype-phenotype correlation for              <i>GLI3<\/i> mutations. Eur J Hum Genet          2015;23: 92\u2013102.","DOI":"10.1038\/ejhg.2014.62"},{"key":"5","doi-asserted-by":"crossref","unstructured":"5. Freese,              K, Driess,                S,                Bornholdt,              D, Shoenle,                EJ, Seidel,                H,                Tinschert,              S, et al.            Gene symbol: <i>GLI3<\/i>. Disease: Pallister-Hall            syndrome. Hum Genet          2003;112: 103.","DOI":"10.1007\/s00439-002-0868-2"},{"key":"6","doi-asserted-by":"crossref","unstructured":"6. Gannag\u00e9-Yared,                MH, Dod\u00e9,                C, Ghanem,                I, Chouery,                E, Jalkh,                N,              Hardelin, JP,              et al. Coexistence of Kallmann syndrome and            complete androgen insensitivity in the same patient. Eur J            Endocrinol          2005;152: 813\u20137.","DOI":"10.1530\/eje.1.01915"},{"key":"7","doi-asserted-by":"crossref","unstructured":"7. Johnson,                EK,                Rosoklija,              I, Shurba,                A, D\u2019Oro,                A, Gordon,                EJ, Chen,                D, et al.            Future fertility for individuals with differences of sex development:            Parent attitudes and perspectives about decision-making. J            Pediatr Urol          2017;13: 402\u201313.","DOI":"10.1016\/j.jpurol.2017.06.002"},{"key":"8","doi-asserted-by":"crossref","unstructured":"8. Kang,              S, Graham,                JM, Olney,                AH,                Biesecker,              LG.              <i>GLI3<\/i> frameshift mutations cause autosomal dominant            Pallister-Hall syndrome. Nat Genet          1997;15: 266\u20138.","DOI":"10.1038\/ng0397-266"},{"key":"9","unstructured":"9. Talsania,                M, Sharma,                R, Sughrue,                ME,                Scofield,              RH, Lim,                J. 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