Comorbidities associated with genetic abnormalities in children with intellectual disability

Intellectual disability (ID) has emerged as the commonest manifestation of underlying genomic abnormalities. Given that molecular genetic tests for diagnosis of ID usually require high costs and yield relatively low diagnostic rates, identification of additional phenotypes or comorbidities may incre...

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Detalles Bibliográficos
Autores principales: Chen, Jia-Shing, Yu, Wen-Hao, Tsai, Meng-Che, Hung, Pi-Lien, Tu, Yi-Fang
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group UK 2021
Materias:
Article
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7985145/
https://www.ncbi.nlm.nih.gov/pubmed/33753861
http://dx.doi.org/10.1038/s41598-021-86131-3

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7985145/
https://www.ncbi.nlm.nih.gov/pubmed/33753861
http://dx.doi.org/10.1038/s41598-021-86131-3

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