1. Andria, G., Ballabio, A., and Parenti, G., 1987, X-linked ichthyosis due to steroid sulfatase deficiency associated with hypogonadism and anosmia, Ann. Neurol.
22:98.
2. Ariturk, E., Tosyali, N., and Ariturk, N., 1992, A case of Waardenburg syndrome and aganglionosis, Turk. J. Pediatr.
34:111–114.
3. Asher, J.H., Jr., Morell, R., and Friedman, T.B., 1991, Waardenburg syndrome (WS): The analysis of a single family with a WS1 mutation showing linkage to RFLP markers on human chromosome 2q, Am. J. Hum. Genet.
48:43–52.
4. Baldwin, C.T., Hoth, C.F., Amos, J. A., Da Silva, E.O., and Milunsky, A., 1992, An exonic mutation in the HuP2 paired domain gene causes Waardenburg syndrome, Nature
355:637–638.
5. Barr, F.G., Galili, N., Holick, J., Biegelo, J.A., Rovera, G., and Emanuel, B.S., 1993, Rearrangement of the PAX3 paired box gene in the pediatric solid tumor alveolar rhabdomyosarcoma, Nature Genetics
3:113–117.