Nizon, M., Henry, M., Michot, C., Baumann, C., Bazin, A., Bessières, B., Blesson, S., Cordier‐Alex, M., David, A., Delahaye‐Duriez, A., Delezoïde, A., Dieux‐Coeslier, A., Doco‐Fenzy, M., Faivre, L., Goldenberg, A., Layet, V., Loget, P., Marlin, S., Martinovic, J., Odent, S., Pasquier, L., Plessis, G., Prieur, F., Putoux, A., Rio, M., Testard, H., Bonnefont, J., & Cormier‐Daire, V. (2016). a series of 38 novel germline and somatic mutations of NIPBL in Cornelia de Lange syndrome. Clinical genetics, 89(5), 584–589. http://access.bl.uk/ark:/81055/vdc_100032018433.0x000051