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Harbuz, R. et al. (n.d.). Osteogenesis imperfecta, tricho‐dento‐osseous syndrome and intellectual disability: A familial case with 17q21.33‐q22 (COL1A1 and DLX3) deletion and 7q32.3‐q33 duplication resulting from a reciprocal interchromosomal insertion. American journal of medical genetics. 161 (10), pp. 2504-2511. [Online].