Analysis of genetic characteristics of 436 children with dysplasia and detailed analysis of rare karyotype
Chromosomal abnormality is one of the important causes of dysplasia in children. However, due to regional and ethnic differences, the reported rates of chromosomal abnormalities in patients with dysplasia vary greatly. Moreover, the clinical manifestations in children with rare chromosomal diseases...
| Hlavní autoři: | , , , , |
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| Médium: | Článek |
| Jazyk: | English |
| Vydáno: |
De Gruyter
2022-04-01
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| Edice: | Open Life Sciences |
| Témata: | |
| On-line přístup: | https://doi.org/10.1515/biol-2022-0046 |