Cite
APA Citation
Harbuz, R., Bilan, F., Couet, D., Charraud, V., Kitzis, A., & Gilbert‐Dussardier, B. (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), 2504–2511. http://access.bl.uk/ark:/81055/vdc_100024734803.0x000016