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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… Expand
National Institutes of Health

Papers overview

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Review
2008
Review
2008
  • L. Biesecker
  • Orphanet journal of rare diseases
  • 2008
  • Corpus ID: 8828318
The Greig cephalopolysyndactyly syndrome (GCPS) is a pleiotropic, multiple congenital anomaly syndrome. It is rare, but precise… Expand
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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… Expand
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Highly Cited
2004
Highly Cited
2004
The cerebellum consists of a highly organized set of folia that are largely generated postnatally during expansion of the granule… Expand
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Highly Cited
2002
Highly Cited
2002
Most current models propose Sonic hedgehog (Shh) as the primary determinant of anteroposterior development of amniote limbs. Shh… Expand
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Highly Cited
2001
Highly Cited
2001
The rational function model (RFM) has gained considerable interest recently mainly due to the fact that Space Imaging Inc… Expand
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Highly Cited
1999
Highly Cited
1999
A combination of phase-shift with gray-code light projection into a three-dimensional vision system based on the projection of… Expand
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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… Expand
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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… Expand
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Highly Cited
1993
Highly Cited
1993
Greig cephalopolysyndactyly syndrome (GCPS) is an autosomal dominant disorder affecting limb and craniofacial development… Expand
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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… Expand
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