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Weill-Marchesani Syndrome, Autosomal Dominant

Known as: MESODERMAL DYSMORPHODYSTROPHY, CONGENITAL, GEMSS, Glaucoma-Lens Ectopia-Microspherophakia-Stiffness-Shortness Syndrome 
The autosomal dominant form of Weill-Marchesani syndrome is associated with Adamts10 gene mutations.
National Institutes of Health

Papers overview

Semantic Scholar uses AI to extract papers important to this topic.
Review
2019
Review
2019
The National Institute of Standards and Technology is in the process of selecting one or more public-key cryptographic algorithms… Expand
2017
2017
The purpose of this document is to present GeMSS : a Great Multivariate Signature Scheme. As suggested by its name, GeMSS is a… Expand
Review
2013
Review
2013
Abstract Hereditary ectopia lentis or lens subluxation can occur with and without systemic associations. Significant overlap can… Expand
Highly Cited
2012
Highly Cited
2012
Latent transforming growth factor (TGF) beta‐binding protein 2 (LTBP2) is an extracellular matrix (ECM) protein that associates… Expand
Highly Cited
2005
Highly Cited
2005
OBJECTIVES The European GEMSS Project is concerned with the creation of medical Grid service prototypes and their evaluation in a… Expand
2005
2005
OBJECTIVES The GEMSS project is developing a secure Grid infrastructure through which six medical simulations services can be… Expand
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Highly Cited
2003
Highly Cited
2003
Sterile mycelia isolated from Pinus tabulaeformis were grouped into white morphotype strains based on cultural characteristics… Expand
2003
2003
Objectives: Grid Enabled Medical Simulation Services (GEMSS) aims to provide a health-computing Grid platform suited to the… Expand
2003
2003
As the Internet revolutionised access to information, the Grid will revolutionise access to computer applications and software… Expand
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1992
1992
We report on a syndrome of progressive joint stiffness, glaucoma, and lens dislocation observed in three generations and compare… Expand