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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.
2013
2013
Waardenburg Syndrome (WS) is an autosomal-dominant disorder characterized by sensorineural hearing loss and pigmentary… Expand
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2011
2011
Waardenburg Syndrome (WS) is a rare hereditary disorder that is characterized by the clinical manifestations of oculocutaneous… Expand
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2009
2009
Glomuvenous malformations are a subtype of venous malformations, which present in infancy or childhood. We describe a teenage… Expand
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2008
2008
A screening program to detect Waardenburg syndrome (WS) conducted between 2002 and 2005, among 1,763 deaf individuals throughout… Expand
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2002
2002
Waardenburg's Syndrome {WS} is described in two girls of a Nigerian family. Both girls presented with white forelock… Expand
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2001
2001
Editor—Hirschsprung disease and Waardenburg syndrome are congenital malformations involving neural crest derivatives. Several… Expand
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1998
1998
This study included 45 unaffected animals and 593 animals affected with heterochromia irides, and 85 enucleated eyeballs with… Expand
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Review
1995
Review
1995
The Waardenburg syndrome (WS) consists of at least two distinct autosomal dominant hereditary disorders. WS Type I has been… Expand
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1983
1983
Daily or twice daily prostaglandin E2 (PGE2) application to cat eyes was shown to maintain a reduced intraocular pressure (IOP… Expand
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1969
1969
Waardenburg-Klein syndrome consists of lateral displacement of the inner canthi of the eyes (dystopia canthorum), a broad nasal… Expand
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