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

Ella M.M.A. Martin, Annabelle Enriquez, Duncan B. Sparrow, David T. Humphreys, Aideen M. McInerney-Leo, Paul J. Leo, Emma L. Duncan, Kavitha R. Iyer, Joelene A. Greasby, Eddie Ip, Eleni Giannoulatou, Delicia Sheng, Elizabeth Wohler, Clémantine Dimartino, Jeanne Amiel, Yline Capri, Daphné Lehalle, Adi Mory, Yael Wilnai, Yael LebenthalAli G. Gharavi, Grazyna G. Krzemień, Monika Miklaszewska, Robert D. Steiner, Cathy Raggio, Robert Blank, Hagit Baris Feldman, Hila Milo Rasouly, Nara L.M. Sobreira, Rebekah Jobling, Christopher T. Gordon, Philip F. Giampietro, Sally L. Dunwoodie, Gavin Chapman

Research output: Contribution to journal › Article › peer-review

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Medicine & Life Sciences