Heterozygous loss of WBP11 function causes multiple congenital defects in humans and mice by Martin, E, Enriquez, A, Sparrow, D, Humphreys, D, McInerney-Leo, A, Leo, P, Duncan, E, Iyer, K, Greasby, J, Ip, E, Giannoulatou, E, Sheng, D, Wohler, E, Dimartino, C, Amiel, J, Capri, Y, Lehall, D, Mory, A, Wilnai, Y, Lebenthal, Y, Gharavi, A, Krzemień, G, Miklaszewska, M, Steiner, R, Raggio, C, Blank, R, Feldman, H, Rasouly, H, Sobreira, N, Jobling, R, Gordon, C, Giampietro, P, Dunwoodie, S, Chapman, G