Clinical characterization of chromosome 5q21.1–21.3 microduplication: A case report

Chromosomal microdeletions and microduplications likely represent the main genetic etiologies for children with developmental delay or intellectual disability. Through prenatal chromosomal microarray analysis, some microdeletions or microduplications can be detected before birth to avoid unnecessary...

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Detalles Bibliográficos
Autores principales: Chen, Shuang, Yu, Yang, Zhang, Han, Li, Leilei, Jiang, Yuting, Liu, Ruizhi, Zhang, Hongguo
Formato: Online Artículo Texto
Lenguaje:English
Publicado: De Gruyter 2020
Materias:
Case Report
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7718637/
https://www.ncbi.nlm.nih.gov/pubmed/33336067
http://dx.doi.org/10.1515/med-2020-0199

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7718637/
https://www.ncbi.nlm.nih.gov/pubmed/33336067
http://dx.doi.org/10.1515/med-2020-0199

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