Author:
Chen Dezhong,Zhao Na,Wang Jing,Li Zhuoyu,Wu Changxin,Fu Jie,Xiao Han
Publisher
Springer Science and Business Media LLC
Subject
Genetics,Molecular Biology,Biochemistry
Reference20 articles.
1. Read AP, Newton VE . Waardenburg syndrome. J Med Genet 1997; 34: 656–665.
2. Baldwin CT, Hoth CF, Macina RA, Milunsky A . Mutations in PAX3 that cause Waardenburg syndrome type I: ten new mutations and review of the literature. Am J Med Genet 1995; 58: 115–122.
3. Eigelshoven S, Kameda G, Kortum AK, Hubsch S, Angerstein W, Singh P et al. Waardenburg syndrome type I with heterochromia iridis and circumscribed hypopigmentation of the skin. Pediatr Dermatol 2009; 26: 759–761.
4. Pardono E, van Bever Y, van den Ende J, Havrenne PC, Iughetti P, Maestrelli SR et al. Waardenburg syndrome: clinical differentiation between types I and II. Am J Med Genet A 2003; 117A: 223–235.
5. Waardenburg PJ . A new syndrome combining developmental anomalies of the eyelids, eyebrows and nose root with pigmentary defects of the iris and head hair and with congenital deafness. Am J Hum Genet 1951; 3: 195–253.
Cited by
6 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