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Transcriptional profiling at the DLK1/MEG3 domain explains clinical overlap between imprinting disorders
Imprinting disorders (IDs) often affect growth in humans, leading to diseases with overlapping features, regardless of the genomic region affected. IDs related to hypomethylation of the human 14q32.2 region and its DLK1/MEG3 domain are associated with Temple syndrome (TS14). TS14 is a rare type of g...
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Publicado no: | Sci Adv |
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Main Authors: | , , , , , , , , , , |
Formato: | Artigo |
Idioma: | Inglês |
Publicado em: |
American Association for the Advancement of Science
2019
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Assuntos: | |
Acesso em linha: | https://ncbi.nlm.nih.gov/pmc/articles/PMC6382400/ https://ncbi.nlm.nih.gov/pubmed/30801013 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1126/sciadv.aau9425 |
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