Dworschak, G. C., Draaken, M., Marcelis, C., de Blaauw, I., Pfundt, R., van Rooij, I. A., Bartels, E., Hilger, A., Jenetzky, E., Schmiedeke, E., Grasshoff‐Derr, S., Schmidt, D., Märzheuser, S., Hosie, S., Weih, S., Holland‐Cunz, S., Palta, M., Leonhardt, J., Schäfer, M., Kujath, C., Rißmann, A., Nöthen, M. M., Zwink, N., Ludwig, M., & Reutter, H. (n.d.). de novo 13q deletions in two patients with mild anorectal malformations as part of VATER/VACTERL and VATER/VACTERL‐like association and analysis of EFNB2 in patients with anorectal malformations. American journal of medical genetics, 161(12), 3035–3041. http://access.bl.uk/ark:/81055/vdc_100024735967.0x000035