2q31.1

Part of the chromosome bands present on the long (q) arm of chromosome 2.
National Institutes of Health

Topic mentions per year

Topic mentions per year

1995-2018
024619952018

Papers overview

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2013
2013
Sex and genetic variation influence the risk of developing diabetic nephropathy and ESRD in patients with type 1 diabetes. We… (More)
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2011
2011
INTRODUCTION The clinical phenotype of the chromosome 2q31 deletion syndrome consists of limb anomalies ranging from… (More)
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2010
2010
Microdeletions of the 2q31.1 region are rare. We present the clinical and molecular findings of eight previously unreported… (More)
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2010
2010
A three-generation family with four patients affected by a novel mesomelic dysplasia was investigated for genome-wide DNA copy… (More)
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2010
2010
In a 19-year-old severely autistic and mentally retarded girl, a balanced de novo t(14;21)(q21.1;p11.2) translocation was found… (More)
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2010
2010
Background: Deletions that encompass 2q31.1 have been proposed as a microdeletion syndrome with common clinical features… (More)
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2009
2009
HOXD gene cluster maps to chromosome 2q31 and plays a key role in embryonic limb morphogenesis. Mutations of the HOXD13 and… (More)
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Highly Cited
2007
Highly Cited
2007
The general lack of pain experience is a rare occurrence in humans, and the molecular causes for this phenotype are not well… (More)
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Highly Cited
2005
Highly Cited
2005
Postmortem brain studies have shown deficits in the cortical γ-aminobutyric acid (GABA) system in schizophrenic individuals… (More)
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2005
2005
We have screened 143 Sicilian (Italian) families with one autistic child to verify, by a linkage disequilibrium approach, the… (More)
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