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Heterozygous loss of WBP11 function causes multiple congenital defects in humans and mice

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.