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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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書目詳細資料
Main Authors: Reis, Linda M, Tyler, Rebecca C, Zori, Roberto, Burgesst, Jennifer, Mueller, Jennifer, Semina, Elena V
格式: Artigo
語言:Inglês
出版: 2013
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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