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The phenotypic spectrum of Xia-Gibbs syndrome
Xia-Gibbs syndrome (XGS: OMIM # 615829) results from de novo truncating mutations within the AT-Hook DNA Binding Motif Containing 1 gene (AHDC1). To further define the phenotypic and molecular spectrum of this disorder, we established an XGS Registry and recruited patients from a worldwide pool of a...
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| 發表在: | Am J Med Genet A |
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| Main Authors: | , , , , , , , , , , , , , |
| 格式: | Artigo |
| 語言: | Inglês |
| 出版: |
2018
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| 主題: | |
| 在線閱讀: | https://ncbi.nlm.nih.gov/pmc/articles/PMC6231716/ https://ncbi.nlm.nih.gov/pubmed/29696776 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1002/ajmg.a.38699 |
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