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Van Lierde, A., Menni, F., Bedeschi, M. F., Natacci, F., Guez, S., Vizziello, P., Costantino, M. A., Lalatta, F., & Esposito, S. (n.d.). healthcare transition in patients with rare genetic disorders with and without developmental disability: Neurofibromatosis 1 and williams–beuren syndrome. American journal of medical genetics, 161(7), 1666–1674. http://access.bl.uk/ark:/81055/vdc_100024733641.0x00000c