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Corrigendum: The Complexities in Genotyping of Congenital Adrenal Hyperplasia: 21-Hydroxylase Deficiency
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| 發表在: | Front Endocrinol (Lausanne) |
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| Main Authors: | , , , , , |
| 格式: | Artigo |
| 語言: | Inglês |
| 出版: |
Frontiers Media S.A.
2020
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| 主題: | |
| 在線閱讀: | https://ncbi.nlm.nih.gov/pmc/articles/PMC7065038/ https://ncbi.nlm.nih.gov/pubmed/32194508 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.3389/fendo.2020.00113 |
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