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IRIDOGONIODYSGENESIS, TYPE 2

Known as: Iridogoniodysgenesis type 2, Iris Hypoplasia With Early-Onset Glaucoma, Autosomal Dominant, ASGD4 
 
National Institutes of Health

Papers overview

Semantic Scholar uses AI to extract papers important to this topic.
2017
2017
Les memoires flash sont integrees dans presque tous les aspects de la vie moderne car leurs uns et zeros representent les donnees… Expand
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2013
2013
This qualitative case study in a rural school in Umgungundlovu District in KwaZulu-Natal, South Africa, explored Grade 12… Expand
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2012
2012
The use of medicine in treating diseases is an integral component of health care, and currently practicing physicians are being… Expand
2008
2008
A rare case is presented of iridogoniodysgenesis syndrome, an autosomal dominant inheritance disorder that includes abnormalities… Expand
2002
2002
This article describes how the school of chemical engineering and advanced materials at Newcastle University is providing new… Expand
Highly Cited
2000
Highly Cited
2000
The autosomal dominant disorders iris hypolasia (IH), iridogoniodysgenesis syndrome (IGDS) and Axenfeld-Rieger syndrome (ARS) are… Expand
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2000
2000
The Bar subclass of homeodomain proteins was first identified for its role in Drosophila eye development. The Bar subclass… Expand
Review
2000
Review
2000
  • W. L. Alward
  • American journal of ophthalmology
  • 2000
  • Corpus ID: 1452913
PURPOSE To review the molecular genetics of Axenfeld-Rieger syndrome and related phenotypes and to discuss how this information… Expand
1999
1999
Iridogoniodysgenesis is an autosomal dominant disorder in which there are abnormalities in the development of the iris stroma and… Expand
Highly Cited
1998
Highly Cited
1998
Axenfeld-Rieger syndrome (ARS) and iridogoniodysgenesis syndrome (IGDS) are clinically related autosomal dominant disorders which… Expand
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