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Journal of Medical Genetics|January 30, 2024
Expanding the phenotype of Kleefstra syndrome: speech, language and cognition in 103 individualsLottie D Morison, Milou G P Kennis, Dmitrijs Rots, et al.Journal of Medical Genetics|November 3, 2022
In-depth characterisation of a cohort of individuals with missense and loss-of-function variants disrupting FOXP2Lottie D Morison, Elisabeth Meffert, Miriam Stampfer, et al.Genetics in Medicine : Official Journal of the American College of Medical Genetics|January 24, 2026
International Clinical Evidence-based Guideline for Kleefstra SyndromeArianne Bouman, Charlotte M W Gaasterland, Carla Sloof-Enthoven, et al.Pageof 2