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    De novo mutations in FBRSL1 cause a novel recognizable malformation and intellectual disability syndrome

    De novo mutations in FBRSL1 cause a novel recognizable malformation and intellectual disability syndrome 由 Ufartes, Roser, Berger, Hanna, Till, Katharina, Salinas, Gabriela, Sturm, Marc, Altmüller, Janine, Nürnberg, Peter, Thiele, Holger, Funke, Rudolf, Apeshiotis, Neophytos, Langen, Hendrik, Wollnik, Bernd, Borchers, Annette, Pauli, Silke

    出版 2020
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