Skip to search formSkip to main contentSkip to account menu

Greig cephalopolysyndactyly syndrome

Known as: Polysyndactyly with peculiar skull shape, Greig syndrome, greigs syndrome 
An autosomal dominant genetic disorder caused by mutations in the GLI3 gene. It is characterized by physical abnormalities of the fingers and/or toes… 
National Institutes of Health

Papers overview

Semantic Scholar uses AI to extract papers important to this topic.
2020
2020
  • 2020
  • Corpus ID: 196624855
Greig cephalopolysyndactyly syndrome is a disorder that affects development of the limbs, head, and face. The features of this… 
2014
2014
Greig cephalopolysyndactyly syndrome is characterized by macrocephaly with a broad and prominent forehead and polysyndactyly… 
2013
2013
The Greig cephalopolysyndactyly syndrome (GCPS) is a rare, autosomal dominant, pleiotropic, multiple congenital anomaly syndrome… 
2006
2006
In this paper the sensor model evaluation and DEM generation for CARTOSAT-1 pan stereo data is described. The model is tested on… 
Review
2005
Review
2005
SUMMARY This paper presents two mathematical models for stereo IKONOS imagery restitution and summarizes the results of their… 
2004
2004
ASTER acquires along track stereoscopic imagery, with a spatial resolution of 15 meters. Automatic generation of Digital… 
Review
2004
Review
2004
Optical stereo and Interferometric Synthetic Aperture Radar (InSAR) techniques were used to process the IRS-1C PAN stereo and ERS… 
1985
1985
A female newborn of healthy parents demonstrates the combination of postaxial hexadactyly type B of the hands (X-ray… 
1982
1982
A father and his son and daughter had preaxial and postaxial polydactyly, syndactyly, and craniofacial changes including… 
1979
1979
Based on the family presented and five others previously described, it can be concluded that the Grieg cephalopolysyndactyly…