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Novel familial distal imprinting centre 1 (11p15.5) deletion provides further insights in imprinting regulation
BACKGROUND: Deletions of the imprinting centre 1 (IC1) in 11p15.5 are rare and their clinical significance is not only influenced by their parental origin but also by their exact genomic localization. In case the maternal IC1 allele is affected, the deletion is associated with the overgrowth disorde...
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| 出版年: | Clin Epigenetics |
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| 主要な著者: | , , , , , |
| フォーマット: | Artigo |
| 言語: | Inglês |
| 出版事項: |
BioMed Central
2019
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| 主題: | |
| オンライン･アクセス: | https://ncbi.nlm.nih.gov/pmc/articles/PMC6377752/ https://ncbi.nlm.nih.gov/pubmed/30770769 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1186/s13148-019-0629-x |
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