Skip to search formSkip to main content
You are currently offline. Some features of the site may not work correctly.

heterochromia of hair

Known as: hair heterochromia 
 
National Institutes of Health

Papers overview

Semantic Scholar uses AI to extract papers important to this topic.
2013
2013
Waardenburg Syndrome (WS) is an autosomal-dominant disorder characterized by sensorineural hearing loss and pigmentary… Expand
  • figure 1
  • figure 2
  • table 1
  • figure 3
  • table 2
2011
2011
Waardenburg Syndrome (WS) is a rare hereditary disorder that is characterized by the clinical manifestations of oculocutaneous… Expand
2009
2009
Glomuvenous malformations are a subtype of venous malformations, which present in infancy or childhood. We describe a teenage… Expand
2008
2008
A screening program to detect Waardenburg syndrome (WS) conducted between 2002 and 2005, among 1,763 deaf individuals throughout… Expand
Review
2003
Review
2003
PURPOSE To determine the visual characteristics of Japanese subjects with the Waardenburg syndrome type 2. METHODS The visual… Expand
  • table 1
  • figure 1
  • figure 2
  • figure 3
  • figure 4
2002
2002
Waardenburg's Syndrome {WS} is described in two girls of a Nigerian family. Both girls presented with white forelock… Expand
2001
2001
Editor—Hirschsprung disease and Waardenburg syndrome are congenital malformations involving neural crest derivatives. Several… Expand
1998
1998
This study included 45 unaffected animals and 593 animals affected with heterochromia irides, and 85 enucleated eyeballs with… Expand
Review
1995
Review
1995
The Waardenburg syndrome (WS) consists of at least two distinct autosomal dominant hereditary disorders. WS Type I has been… Expand
1983
1983
Daily or twice daily prostaglandin E2 (PGE2) application to cat eyes was shown to maintain a reduced intraocular pressure (IOP… Expand