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heterochromia of hair

Known as: hair heterochromia 
National Institutes of Health

Papers overview

Semantic Scholar uses AI to extract papers important to this topic.
2011
2011
Waardenburg Syndrome (WS) is a rare hereditary disorder that is characterized by the clinical manifestations of oculocutaneous… 
Review
2010
Review
2010
Waardenburg syndrome (WS) is characterized by the association of pigmentation abnormalities, including depigmented patches of the… 
2008
2008
A screening program to detect Waardenburg syndrome (WS) conducted between 2002 and 2005, among 1,763 deaf individuals throughout… 
Review
2006
Review
2006
Objective: Waardenburg syndrome is an autosomal‐dominant syndrome characterized by dystopia canthorum, hyperplasia of the… 
Highly Cited
2001
Highly Cited
2001
Editor—Hirschsprung disease and Waardenburg syndrome are congenital malformations involving neural crest derivatives. Several… 
1998
1998
This study included 45 unaffected animals and 593 animals affected with heterochromia irides, and 85 enucleated eyeballs with… 
Review
1995
Review
1995
The Waardenburg syndrome (WS) consists of at least two distinct autosomal dominant hereditary disorders. WS Type I has been… 
1983
1983
Daily or twice daily prostaglandin E2 (PGE2) application to cat eyes was shown to maintain a reduced intraocular pressure (IOP…