Clinical phenotype of FOXP1 syndrome: parent-reported medical signs and symptoms in 40 individuals
Koene, Saskia, Ropers, Fabiënne Gwendolin, Wieland, Jannelien, Rybak, Tamara, Wildschut, Floor, Berghuis, Dagmar, Morgan, Angela, Trelles, Maria Pilar, Scheepe, Jeroen Ronald, Bökenkamp, Regina, Peeters-Scholte, Cacha M P C D, Braden, Ruth, Santen, Gijs W E
Published in Journal of medical genetics (21.03.2024)
Published in Journal of medical genetics (21.03.2024)
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