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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

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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
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2012
2012
Latent transforming growth factor (TGF) beta-binding protein 2 (LTBP2) is an extracellular matrix (ECM) protein that associates… Expand
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2008
2008
The first part of this paper presents a selection of medical simulation applications, including image reconstruction, near real… Expand
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2005
2005
OBJECTIVES The European GEMSS Project is concerned with the creation of medical Grid service prototypes and their evaluation in a… Expand
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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
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2003
2003
Objectives: Grid Enabled Medical Simulation Services (GEMSS) aims to provide a health-computing Grid platform suited to the… Expand
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2003
2003
As the Internet revolutionised access to information, the Grid will revolutionise access to computer applications and software… Expand
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2003
2003
The central objective of the SimBio project is the improvement of clinical and medical practices by the use of large-scale… 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
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