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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 mā 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

    I whakaputaina 2020
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