X-chromosome inactivation: implications in human disease
Author:
Publisher
Springer Science and Business Media LLC
Subject
Genetics
Link
https://link.springer.com/content/pdf/10.1007/s12041-021-01314-1.pdf
Reference27 articles.
1. Aarabi M., Kessler E., Madan-Khetarpal S., Surti U., Bellissimo D., Rajkovic A. et al. 2019 Autism spectrum disorder in females with ARHGEF9 alterations and a random pattern of X chromosome inactivation. Eur. J. Med. Genet. 62, 239–242.
2. Berletch J. B., Yang F., Xu J., Carrel L. and Disteche C. M. 2011 Genes that escape from X inactivation. Hum. Genet. 130, 237–245.
3. Bicocchi M. P., Migeon B. R., Pasino M., Lanza T., Bottini F., Boeri E. et al. 2005 Familial nonrandom inactivation linked to the X inactivation centre in heterozygotes manifesting haemophilia A. Eur. J. Hum. Genet. 13, 635–640.
4. Blaschke R. J. and Rappold G. 2006 The pseudoautosomal regions, SHOX and disease. Curr. Opin. Genet. Dev. 16, 233–239.
5. Cantone I. and Fisher A. G. 2017 Human X chromosome inactivation and reactivation: implications for cell reprogramming and disease. Philos. Trans. R. Soc. London B Biol. Sci. 372, 20160358.
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