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Original Articles

Facial clues to an inherited syndrome

, MD
Pages 107-110 | Published online: 30 Jun 2015

References

  • 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
  • Fitzpatrick's dermatology in general medicine (book on CDROM). Version 1. Based on: Freedberg IM, Eisen AZ, Wolff K, et al, eds. Fitzpatrick's dermatology in general medicine. 5th ed. New York: McGraw-Hill, 1999
  • Grundfast KM, San Agustin TB. Finding the gene(s) for Waardenburg syndrome(s). Otolaryngol Clin North Am 1992; 25(5): 935–51
  • Farrer LA, Arnos KS, Asher JH Jr, et al. Locus heterogeneity for Waardenburg syndrome is predictive of clinical subtypes. Am J Hum Genet 1994; 55(4): 728–37
  • Desch LW. White forelock could be early sign of tuberous sclerosis. Arch Pediatr Adolesc Med 1996; 150(6): 651–2

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