Clinical and genetic analysis of a phenotypically normal three-generation family carrying 10.884 Mb deletions at 13q21.1q21.32
Objective: Patients with variations exhibiting abnormal phenotypes or no significant clinical signs offer crucial insights into our genome's complexities. To help determine the pathogenicity of 13q21.1q21.32 deletion, we reported four patients in a family carrying this variation. Case report: Our st...
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| Hlavní autoři: | , , , , , , |
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| Médium: | Artigo |
| Jazyk: | Inglês |
| Vydáno: |
Elsevier
2026-07-01
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| Edice: | Taiwanese Journal of Obstetrics & Gynecology |
| Témata: | |
| On-line přístup: | http://www.sciencedirect.com/science/article/pii/S1028455926001713 |
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