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Wilson,              LC, Leverton,                K, Oude                Luttikhuis, ME,                Oley, CA,                Flint, J,                Wolstenholme,              J, et al.            Brachydactyly and mental retardation: an Albright hereditary            osteodystrophy-like syndrome localized to 2q37. Am J Hum            Genet          1995;56: 400\u20137."},{"key":"2","doi-asserted-by":"crossref","unstructured":"2. Le,                TN,                Williams,              SR, Alaimo,                JT, Elsea,                SH. Genotype            and phenotype correlation in 103 individuals with 2q37 deletion syndrome reveals            incomplete penetrance and supports HDAC4 as the primary genetic            contributor. Am J Med Genet A          2019;179: 782\u201391.","DOI":"10.1002\/ajmg.a.61089"},{"key":"3","doi-asserted-by":"crossref","unstructured":"3. Wheeler,                PG, Huang,                D, Dai,                Z.            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