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D Morison

Showing results (11-20 of 19) with videos related to

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European Journal of Medical Genetics|February 12, 2024
Beyond 'speech delay': Expanding the phenotype of BRPF1-related disorderLottie D Morison, Olivia Van Reyk, Emma Baker, et al.
Developmental Medicine and Child Neurology|January 23, 2025
Adaptive functioning in children and young adults with monogenic neurodevelopmental disordersEmma K Baker, Miya St John, Ruth Braden, et al.
American Journal of Medical Genetics. Part B, Neuropsychiatric Genetics : the Official Publication of the International Society of Psychiatric Genetics|February 29, 2024
Speech and language in DDX3X-neurodevelopmental disorder: A call for early augmentative and alternative communication interventionElana J Forbes, Lottie D Morison, Fatma Lelik, et al.
Journal of Inherited Metabolic Disease|January 17, 2025
Speech, Language and Non-verbal Communication in CLN2 and CLN3 Batten DiseaseLottie D Morison, Ineka T Whiteman, Adam P Vogel, et al.
European Journal of Human Genetics : EJHG|May 16, 2025
Understanding speech and language in KIF1A-associated neurological disorderLottie D Morison, Adam P Vogel, John Christodoulou, et al.
European Journal of Human Genetics : EJHG|January 4, 2023
CDK13-related disorder: a deep characterization of speech and language abilities and addition of 33 novel casesLottie D Morison, Olivia van Reyk, Elana Forbes, et al.
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 <i>FOXP2</i>Lottie 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

Showing results (11-20 of 19) with videos related to

Sort By:
Pageof 2
You have reached the last page of results.This site can display upto 19 results.
European Journal of Medical Genetics|February 12, 2024
Beyond 'speech delay': Expanding the phenotype of BRPF1-related disorderLottie D Morison, Olivia Van Reyk, Emma Baker, et al.
Developmental Medicine and Child Neurology|January 23, 2025
Adaptive functioning in children and young adults with monogenic neurodevelopmental disordersEmma K Baker, Miya St John, Ruth Braden, et al.
American Journal of Medical Genetics. Part B, Neuropsychiatric Genetics : the Official Publication of the International Society of Psychiatric Genetics|February 29, 2024
Speech and language in DDX3X-neurodevelopmental disorder: A call for early augmentative and alternative communication interventionElana J Forbes, Lottie D Morison, Fatma Lelik, et al.
Journal of Inherited Metabolic Disease|January 17, 2025
Speech, Language and Non-verbal Communication in CLN2 and CLN3 Batten DiseaseLottie D Morison, Ineka T Whiteman, Adam P Vogel, et al.
European Journal of Human Genetics : EJHG|May 16, 2025
Understanding speech and language in KIF1A-associated neurological disorderLottie D Morison, Adam P Vogel, John Christodoulou, et al.
European Journal of Human Genetics : EJHG|January 4, 2023
CDK13-related disorder: a deep characterization of speech and language abilities and addition of 33 novel casesLottie D Morison, Olivia van Reyk, Elana Forbes, et al.
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 <i>FOXP2</i>Lottie 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