A newborn with developmental delay diagnosed with 4q35 deletion and 10p duplication
We report the case of an infant with a 4q35.1 deletion with 10p duplication. This mutation is rarely reported in the literature and has been found to have variable clinical findings, often including developmental delay. In this case, the condition was detected by chromosomal microarray analysis afte...
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| Veröffentlicht in: | Journal of genetic medicine 2020-12, Vol.17 (2), p.102-107 |
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| Hauptverfasser: | , , , |
| Format: | Artikel |
| Sprache: | kor |
| Online-Zugang: | Volltext |
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