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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Bibliographic Details
Published in:Open Med (Wars)
Main Authors: Chen, Shuang, Yu, Yang, Zhang, Han, Li, Leilei, Jiang, Yuting, Liu, Ruizhi, Zhang, Hongguo
Format: Artigo
Language:Inglês
Published: De Gruyter 2020
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Case Report
Online Access:https://ncbi.nlm.nih.gov/pmc/articles/PMC7718637/
https://ncbi.nlm.nih.gov/pubmed/33336067
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1515/med-2020-0199
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