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JACKSON-WEISS SYNDROME

Known as: Acrocephalosyndactyly Jackson Weiss type, Enlarged great toes and craniofacial abnormalities, JWS 
A rare, autosomal dominant inherited disorder caused by mutations in the FGFR2 gene. It is characterized by the premature fusion of the bones of the… Expand
National Institutes of Health

Papers overview

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Highly Cited
2012
Highly Cited
2012
  • Mark Jackson
  • History of the human sciences
  • 2012
  • Corpus ID: 743348
In 1956, Hans Selye tentatively suggested that the scientific study of stress could ‘help us to formulate a precise program of… Expand
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Highly Cited
2012
Highly Cited
2012
We examine whether vocal markers of cognitive dissonance are useful for detecting financial misreporting. We use speech samples… Expand
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Highly Cited
2006
Highly Cited
2006
Abstract The cognitive‐behavioral, fear‐avoidance (FA) model of chronic pain (Vlaeyen JWS, Kole‐Snijders AMJ, Boeren RGB, van Eek… Expand
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Highly Cited
2005
Highly Cited
2005
Building a myofibril from its component proteins requires the interactions of many different proteins in a process whose details… Expand
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Highly Cited
2004
Highly Cited
2004
UNLABELLED JWS Online is a repository of kinetic models, describing biological systems, which can be interactively run and… Expand
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Highly Cited
2003
Highly Cited
2003
Abstract Some of the remaining crucial plasma edge physics and plasma–material interaction issues of the ITER tokamak are… Expand
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Highly Cited
2002
Highly Cited
2002
The validity of two analogous caregiver/parent report measures of early language development in young children who are learning… Expand
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Highly Cited
1995
Highly Cited
1995
Note: Howard Hughes Medical Institute, Department of Chemistry and Biochemistry, University of Colorado, Boulder 80309, USA… Expand
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Highly Cited
1995
Highly Cited
1995
The study compared treatment programs with EEG biofeedback or stimulants as their primary components. An EEG group (EEG) was… Expand
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Highly Cited
1994
Highly Cited
1994
Jackson-Weiss syndrome is an autosomal dominant condition characterized by craniosynostosis, foot anomalies and great phenotypic… Expand
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