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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

Related topics

Related topics

18 relations
Aarskog syndromeAgenesis of corpus callosumAutosomal dominant inheritanceCongenital Camptodactyly

Broader (2)

AcrocephalosyndactyliaPolysyndactyly

Papers overview

Semantic Scholar uses AI to extract papers important to this topic.
Review
2015
Review
2015
Accuracy Assessment in Structure from Motion 3d Reconstruction from Uav-Born Images: the Influence of the Data Processing Methods
Abstract. The evolution of Structure from Motion (SfM) techniques and their integration with the established procedures of… 
2012
2012
CHARACTERISTICS OF VERY HIGH RESOLUTION OPTICAL SATELLITES FOR TOPOGRAPHIC MAPPING
The ground resolution of optical satellites now overlaps with the ground resolution of aerial images. The radiometric and… 
2003
2003
QuickBird...Geometric Correction, Path and Block Processing and Data Fusion
Since the successful launch of DigitalGlobe’s QuickBird satellite and the availability of the data, QuickBird Imagery has quickly… 
2003
2003
Variable phenotype in Greig cephalopolysyndactyly syndrome: Clinical and radiological findings in 4 independent families and 3 sporadic cases with identified GLI3 mutations
Greig cephalopolysyndactyly (GCPS) (OMIM 175700) is an autosomal dominant disorder characterized by a distinct combination of… 
1990
1990
Molecular and cytogenetic analysis in two patients with microdeletions of 7p and Greig syndrome: hemizygosity for PGAM2 and TCRG genes.
Highly Cited
1988
Highly Cited
1988
Greig cephalopolysyndactyly syndrome: a possible mouse homologue (Xt-extra toes).
Greig cephalopolysyndactyly syndrome is an autosomal dominant form of complex polydactyly in man. Attention is called to the… 
Highly Cited
1988
Highly Cited
1988
Chromosomal localisation of a developmental gene in man: direct DNA analysis demonstrates that Greig cephalopolysyndactyly maps to 7p13.
Greig cephalopolysyndactyly syndrome (GCPS) is a rare autosomal dominant form of complex polydactyly. GCPS has been tentatively… 
Review
1985
Review
1985
The Greig cephalopolysyndactyly syndrome: report of a family and review of the literature.
The Greig cephalopolysyndactyly syndrome in characterized by a set of craniofacial defects (macrocephaly, broad nasal root… 
1982
1982
The Greig cephalopolysyndactyly syndrome in a Canadian family.
A father and his son and daughter had preaxial and postaxial polydactyly, syndactyly, and craniofacial changes including… 
1979
1979
Greig cephalopolysyndactyly syndrome.
Based on the family presented and five others previously described, it can be concluded that the Grieg cephalopolysyndactyly… 
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