Roberts-SC phocomelia syndrome

Known as: ROBERTS SYNDROME, Appelt-Gerken-Lenz Syndrome, Sc Syndrome 
A rare genetic syndrome with an autosomal recessive pattern of inheritance. It is caused by a mutation in the ESCO2 gene. Clinical signs at birth… (More)
National Institutes of Health

Papers overview

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Highly Cited
2013
Highly Cited
2013
Nonparametric bootstrap has been a widely used tool in phylogenetic analysis to assess the clade support of phylogenetic trees… (More)
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Highly Cited
2012
Highly Cited
2012
a Digestive Diseases Branch, NIH, Bethesda, Md. , USA; b Service d’Hépato-Gastroentérologie, CHU de Reims, Hôpital Robert Debr… (More)
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Highly Cited
2008
Highly Cited
2008
Despite recent advances achieved by application of high-performance computing methods and novel algorithmic techniques to maximum… (More)
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Highly Cited
2008
Highly Cited
2008
Recent advances in DNA sequencers are accelerating genome sequencing, especially in microbes, and complete and draft genomes from… (More)
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Highly Cited
2005
Highly Cited
2005
Roberts syndrome is an autosomal recessive disorder characterized by craniofacial anomalies, tetraphocomelia and loss of cohesion… (More)
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Highly Cited
2003
Highly Cited
2003
This paper documents the relations between firms’ pre-offer market valuations and takeover behavior, and evaluates their… (More)
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Highly Cited
2000
Highly Cited
2000
This Article is brought to you for free and open access by the Economics at Digital Commons @ Loyola Marymount University and… (More)
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Highly Cited
1992
Highly Cited
1992
HUMAN coronaviruses (HCV) in two serogroups represented by HCV-229E and HCV-OC43 are an important cause of upper respiratory… (More)
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Highly Cited
1991
Highly Cited
1991
Endothelial cells that make up brain capillaries and constitute the blood-brain barrier become different from peripheral… (More)
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1979
1979
Roberts syndrome and SC phocomelia syndrome are an autosomal recessive condition of prenatal and postnatal growth retardation… (More)
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