Clinical phenotype of FOXP1 syndrome: parent-reported medical signs and symptoms in 40 individuals.
Koene S, Ropers FG, Wieland J, Rybak T, Wildschut F, Berghuis D, Morgan A, Trelles MP, Scheepe JR, Bökenkamp R, Peeters-Scholte CMPCD, Braden R, Santen GWE.
Koene S, et al. Among authors: scheepe jr.
J Med Genet. 2024 Mar 21;61(4):399-404. doi: 10.1136/jmg-2023-109537.
J Med Genet. 2024.
PMID: 38123995