Author:
Madden Colm,Halsted Mark J.,Hopkin Robert J.,Choo Daniel I.,Benton Corning,Greinwald John H.
Reference36 articles.
1. 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;Waardenburg;Am J Hum Genet,1951
2. Genetic heterogeneity in Waardenburg syndrome;Arias;Birth Defects,1971
3. Upper limb involvement in the Klein-Waardenburg syndrome;Goodman;Am J Med Genet,1982
4. Historical background and evidence for dominant inheritance of the Klein-Waardenburg syndrome (type III);Klein;Am J Med Genet,1983
5. White forelock, pigmentary disorder of the irides, and long segment Hirschsprung disease: possible variant of Waardenburg syndrome;Shah;J Pediatr,1981
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58 articles.
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