Expanding the speech and language phenotype in Koolen-de Vries syndrome: late onset and periodic stuttering a novel feature.

St John, Miya; van Reyk, Olivia; Koolen, David A; de Vries, Bert B A; Amor, David J; Morgan, Angela T

St John, Miya; van Reyk, Olivia; Koolen, David A; de Vries, Bert B A; Amor, David J; Morgan, Angela T.

Afiliación

St John M; Murdoch Children's Research Institute, Parkville, VIC, Australia.
van Reyk O; Department of Audiology and Speech Pathology, University of Melbourne, Melbourne, VIC, Australia.
Koolen DA; Murdoch Children's Research Institute, Parkville, VIC, Australia.
de Vries BBA; Department of Human Genetics, Radboud Institute for Molecular Life Sciences and Donders Institute for Brain, Cognition and Behaviour, Radboud University Medical Center, Nijmegen, The Netherlands.
Amor DJ; Department of Human Genetics, Radboud Institute for Molecular Life Sciences and Donders Institute for Brain, Cognition and Behaviour, Radboud University Medical Center, Nijmegen, The Netherlands.
Morgan AT; Murdoch Children's Research Institute, Parkville, VIC, Australia.

Eur J Hum Genet ; 31(5): 531-540, 2023 05.

Article en En | MEDLINE | ID: mdl-36529818

Asunto(s)

Discapacidad Intelectual; Tartamudeo; Humanos; Femenino; Discapacidad Intelectual/diagnóstico; Discapacidad Intelectual/genética; Habla; Tartamudeo/diagnóstico; Tartamudeo/genética; Actividades Cotidianas; Fenotipo

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Texto completo: 1 Banco de datos: MEDLINE Asunto principal: Tartamudeo / Discapacidad Intelectual Tipo de estudio: Qualitative_research Límite: Female / Humans Idioma: En Revista: Eur J Hum Genet Asunto de la revista: GENETICA MEDICA Año: 2023 Tipo del documento: Article País de afiliación: Australia

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