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Altered Intra-Nuclear Organisation of Heterochromatin and Genes in ICF Syndrome
The ICF syndrome is a rare autosomal recessive disorder, the most common symptoms of which are immunodeficiency, facial anomalies and cytogenetic defects involving decondensation and instability of chromosome 1, 9 and 16 centromeric regions. ICF is also characterised by significant hypomethylation o...
में बचाया:
| मुख्य लेखकों: | , , , , , , , |
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| स्वरूप: | Artigo |
| भाषा: | Inglês |
| प्रकाशित: |
Public Library of Science
2010
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| विषय: | |
| ऑनलाइन पहुंच: | https://ncbi.nlm.nih.gov/pmc/articles/PMC2894064/ https://ncbi.nlm.nih.gov/pubmed/20613881 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1371/journal.pone.0011364 |
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