File:Waardenburg syndrome type 1.png
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Summary
| Description |
English: Facial appearance of a boy from China with Waardenburg syndrome type 1, caused by a mutation in the PAX3 gene |
| Date | |
| Source |
Ma, J, Lin, K, Jiang, H‐C, et al. A novel mutation of the PAX3 gene in a Chinese family with Waardenburg syndrome type I. Mol Genet Genomic Med. 2019; 7:e798. https://doi.org/10.1002/mgg3.798 Annotated label "(a)" was removed by User:SUM1. |
| Author | Ma, J, Lin, K, Jiang, H‐C, et al. |
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| Date/Time | Thumbnail | Dimensions | User | Comment | |
|---|---|---|---|---|---|
| current | 13:08, 14 December 2019 | | 1,055 × 826 (859 KB) | commons>SUM1 | User created page with UploadWizard |
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