Clinical and genetic study on a cleidocranial dysplasia family
Objective To confirm the mutation in a family with cleidocranial dysplasia (CCD) and explore its possible effects on protein structure and function. Methods A proband with CCD was diagnosed through clinical symptoms and radiography examinations. Peripheral blood samples were collected from the proba...
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| 1. autor: | |
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| Format: | Artigo |
| Język: | Chinês |
| Wydane: |
Editorial Office of Stomatology
2026-01-01
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| Seria: | Kouqiang yixue |
| Hasła przedmiotowe: | |
| Dostęp online: | https://www.stomatology.cn/fileup/1003-9872/PDF/1768555877550-1757776984.pdf |
| Etykiety: |
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