Author:
Sun Lianhua,Li Xiaohua,Shi Jun,Pang Xiuhong,Hu Yechen,Wang Xiaowen,Wu Hao,Yang Tao
Publisher
Springer Science and Business Media LLC
Reference11 articles.
1. Read, A. P. & Newton, V. E. Waardenburg syndrome. Journal of medical genetics 34, 656–665 (1997).
2. Newton, V. Hearing loss and Waardenburg’s syndrome: implications for genetic counselling. J Laryngol Otol 104, 97–103 (1990).
3. Puffenberger, E. G. et al. A missense mutation of the endothelin-B receptor gene in multigenic Hirschsprung’s disease. Cell 79, 1257–1266 (1994).
4. Hoth, C. F. et al. Mutations in the paired domain of the human PAX3 gene cause Klein-Waardenburg syndrome (WS-III) as well as Waardenburg syndrome type I (WS-I). American journal of human genetics 52, 455–462 (1993).
5. Pingault, V. et al. Review and update of mutations causing Waardenburg syndrome. Human mutation 31, 391–406 (2010).
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