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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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| 發表在: | Open Med (Wars) |
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| Main Authors: | , , , , , , |
| 格式: | Artigo |
| 語言: | Inglês |
| 出版: |
De Gruyter
2020
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| 主題: | |
| 在線閱讀: | 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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