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29 year old man with visual symptoms and headaches
Digital Journal of Ophthalmology 1997
Volume 3, Number 14
March 4, 1997
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Yichieh Shiuey, MD | Massachusetts Eye and Ear Infirmary, Harvard Medical School, Boston, MA
References
1) Waardenburg, PJ: A new syndrome combining developmental anomalies of the eyelids, eyebrows, and nose root with pigmentary defects of the iris and headhair and with condgenital deafness. Am J Hum Genet 3:195 (1951)
2) Baldwin CT, Hoth CF, Amos JA et al: An exonic mutation in the HuP2 paired domain gene causes Waardenburg's syndrome. Nature 355:637 (1993)
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