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A Case of 22q11.2 Deletion Syndrome with Peters Anomaly, Congenital Glaucoma, and Heterozygous Mutation in CYP1B1
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| Main Authors: | , , , , , |
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| 格式: | Artigo |
| 語言: | Inglês |
| 出版: |
2013
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| 主題: | |
| 在線閱讀: | https://ncbi.nlm.nih.gov/pmc/articles/PMC4092044/ https://ncbi.nlm.nih.gov/pubmed/24024747 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.3109/13816810.2013.835432 |
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