1. Bondurand, N., Dastot-Le Moal, F., Stanchina, L., et al. (2007). Deletions at the SOX10 gene locus cause Waardenburg syndrome types 2 and 4. American Journal of Human Genetics, 81, 1169–1185.
2. Bondurand, N., Pingault, V., Goerich, D. E., et al. (2000). Interaction among SOX10, PAX3 and MITF, three genes altered in Waardenburg syndrome. Human Molecular Genetics, 9, 1907–1917.
3. Bonnet, J., Pediatr, T. M., Edery, P., et al. (1996). Waardenburg-Hirschsprung disease in two sisters: A possible clue to the genetics of this association? European Journal of Pediatric Surgery, 6, 245–248.
4. Cortés-González, V., Zenteno, J. C., Guzmán-Sánchez, M., et al. (2016). Tietz/Waardenburg type 2A syndrome associated with posterior microphthalmos in two unrelated patients with novel MITF gene mutations. American Journal of Medical Genetics Part A, 9999A, 1–4.
5. Cullen, R. D., Zdanski, C., Roush, P., et al. (2006). Cochlear implants in Waardenburg syndrome. Layngoscope, 116, 1273–1275.