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… (More)
National Institutes of Health

Papers overview

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Review
2008
Review
2008
The Greig cephalopolysyndactyly syndrome (GCPS) is a pleiotropic, multiple congenital anomaly syndrome. It is rare, but precise… (More)
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2008
2008
Greig cephalopolysyndactyly syndrome (GCPS) is a rare multiple congenital anomaly syndrome that is inherited in an autosomal… (More)
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Highly Cited
2005
Highly Cited
2005
Mutations in the GLI3 zinc-finger transcription factor gene cause Greig cephalopolysyndactyly syndrome (GCPS) and Pallister-Hall… (More)
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1999
1999
Greig cephalopolysyndactyly syndrome, characterized by craniofacial and limb anomalies (GCPS; MIM 175700), previously has been… (More)
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Highly Cited
1998
Highly Cited
1998
Nature Genet. 3, 241–246 (1993). Originally, we reported that the 3 ́ end of Gli3 is not deleted in the XtJ allele (Fig. 4). U. R… (More)
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Highly Cited
1997
Highly Cited
1997
Pallister-Hall syndrome (PHS, M146510) was first described in 1980 in six newborns. It is a pleiotropic disorder of human… (More)
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Highly Cited
1993
Highly Cited
1993
Greig cephalopolysyndactyly syndrome (GCPS) is an autosomal dominant disorder affecting limb and craniofacial development… (More)
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1992
1992
The dominant mouse mutant extra toes (Xt) is characterized by preaxial and postaxial polydactyly of the feet and a white belly… (More)
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Highly Cited
1991
Highly Cited
1991
THE Greig cephalopolysyndactyly syndrome (GCPS) is an auto-somal dominant disorder affecting limb and craniofacial development in… (More)
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1979
1979
Based on the family presented and five others previously described, it can be concluded that the Grieg cephalopolysyndactyly… (More)
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