X-Linked Trait
Author:
Publisher
Springer International Publishing
Link
https://link.springer.com/content/pdf/10.1007/978-3-319-55065-7_568
Reference18 articles.
1. Amir, R., Veyver V., Ignatia, Mimi, W., Charles, T., Uta F., Huda Z.(1999). Rett syndrome is caused by mutations in X-linked MECP2, encoding methyl-CpG-binding protein 2. Nature Genetics, 23(2):185–8.
2. Dick, F. D. (2006). Solvent neurotoxicity. Occupational and Environmental Medicine, 63(3), 221.
3. Haemophilia in Queen Victoria’s Descendants. (2006). Wayback machine.
4. Hladnik, U., Nyhan, W. L., & Bertelli, M. (2008). Variable expression of HPRT deficiency in 5 members of a family with the same mutation. Archives of Neurology, 65(9), 1240–1243.
5. Hunter, C. (1917). A rare disease of two brothers. Proceedings of the Royal Society of Medicine, 10(Sect Study Dis Child), 104.
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