Nonrandom X chromosome DNA methylation patterns in hemophiliac females.
Author:
Publisher
American Society for Clinical Investigation
Subject
General Medicine
Cited by 35 articles. 订阅此论文施引文献 订阅此论文施引文献,注册后可以免费订阅5篇论文的施引文献,订阅后可以查看论文全部施引文献
1. Maternal microchimerism protects hemophilia A patients from inhibitor development;Blood Advances;2020-05-06
2. Hemophilia B in a female with intellectual disability caused by a deletion of Xq26.3q28 encompassing the F9;Molecular Genetics & Genomic Medicine;2018-09-27
3. Autoimmune thyroiditis following HLA-matched sibling hematopoietic stem cell transplantation for Wiskott-Aldrich syndrome;Pediatric Transplantation;2018-05-15
4. Phenotype-genotype correlations in hemophilia A carriers are consistent with the binary role of the phase between F8 and X-chromosome inactivation;Journal of Thrombosis and Haemostasis;2015-03-14
5. Androgen receptor CAG repeats, non-random X chromosome inactivation, and loss of heterozygosity at Xq25 in relation to breast cancer risk;BMC Cancer;2014-03-01
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