Skip to search formSkip to main contentSkip to account menu

NHS protein, human

Known as: Nance-Horan syndrome (congenital cataracts and dental anomalies) protein, human, Nance-Horan syndrome protein, human 
National Institutes of Health

Related topics

Related topics

2 relations
NHS gene

Broader (1)

Nuclear Proteins

Papers overview

Semantic Scholar uses AI to extract papers important to this topic.
2008
2008
Nance‐Horan syndrome: a contiguous gene syndrome involving detetion of the ametogenin gene? A case report and molecular analysis
DESIGN: A case of Nance-Horan syndrome in a male is presented, with some features of the condition in his carrier mother and her… 
1995
1995
Nance-Horan syndrome: a contiguous gene syndrome involving deletion of the amelogenin gene? A case report and molecular analysis.
DESIGN A case of Nance-Horan syndrome in a male is presented, with some features of the condition in his carrier mother and her… 
1990
1990
Nance-Horan syndrome: localization within the region Xp21.1-Xp22.3 by linkage analysis.
Nance-Horan Syndrome (NHS) or X-linked cataract-dental syndrome (MIM 302350) is a disease of unknown pathogenesis characterized… 
By clicking accept or continuing to use the site, you agree to the terms outlined in our Privacy Policy (opens in a new tab), Terms of Service (opens in a new tab), and Dataset License (opens in a new tab)