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Children (Basel, Switzerland)|May 28, 2022
The Genetic and Molecular Basis of Developmental Language Disorder: A ReviewHayley S Mountford, Ruth Braden, Dianne F Newbury, et al.American Journal of Medical Genetics. Part A|July 27, 2025
Speech and Language Disorders Associated With 7q31 Deletions Implicating FOXP2Lottie D Morison, Ruth Braden, David J Amor, et al.European Journal of Human Genetics : EJHG|February 2, 2024
The value of genomic testing in severe childhood speech disordersYan Meng, Stephanie Best, David J Amor, et al.Journal of Multidisciplinary Healthcare|April 29, 2024
Clinician Awareness of Stickler Syndromes Among Australian Allied Health Care ProfessionalsAlexis Ceecee Britten-Jones, Lauren N Ayton, Kelley Graydon, et al.Research in Developmental Disabilities|November 1, 2025
Improving prognostication for individuals with FOXP1 syndrome: Parent-reported practical and social skills in 52 individualsSaskia Koene, Marieke Rothuizen-Lindenschot, Fabienne G Ropers, 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.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|April 28, 2021
Speech and language deficits are central to SETBP1 haploinsufficiency disorderAngela Morgan, Ruth Braden, Maggie M K Wong, et al.Journal of Medical Genetics|December 20, 2023
Clinical phenotype of FOXP1 syndrome: parent-reported medical signs and symptoms in 40 individualsSaskia Koene, Fabiënne Gwendolin Ropers, Jannelien Wieland, et al.Pageof 2