DNA methylation signature in peripheral blood reveals distinct characteristics of human X chromosome numerical aberrations
Background Abnormal sex chromosome numbers in humans are observed in Turner (45,X) and Klinefelter (47,XXY) syndromes. Both syndromes are associated with several clinical phenotypes, whose molecular mechanisms are obscure, and show a range of inter-individual penetrance. In order to understand the e...
محفوظ في:
| المؤلف الرئيسي: | El Maarri, Osman (author) |
|---|---|
| مؤلفون آخرون: | Sharma, Amit (author), Jamil, Muhammad Ahmer (author), Nuesgen, Nicole (author), Schreiner, Felix (author), Priebe, Lutz (author), Hoffman, Per (author) |
| التنسيق: | article |
| منشور في: |
2015
|
| الوصول للمادة أونلاين: | http://hdl.handle.net/10725/6198 https://doi.org/10.1186/s13148-015-0112-2 http://libraries.lau.edu.lb/research/laur/terms-of-use/articles.php https://clinicalepigeneticsjournal.biomedcentral.com/articles/10.1186/s13148-015-0112-2 |
| الوسوم: |
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