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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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| Publicado no: | Open Med (Wars) |
|---|---|
| Main Authors: | , , , , , , |
| Formato: | Artigo |
| Idioma: | Inglês |
| Publicado em: |
De Gruyter
2020
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| Assuntos: | |
| Acesso em linha: | 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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