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10q26.2

A chromosome band present on 10q
National Institutes of Health

Papers overview

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2019
2019
Systemic sclerosis (SSc) is a complex, heterogeneous connective tissue disease, characterized by fibrosis and ECM deposition in… Expand
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2017
2017
To identify genomic markers associated with the response to neoadjuvant chemotherapy (NACT) in patients with cervical cancer, we… Expand
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2015
2015
The 10q26 deletion syndrome is a clinically heterogeneous disorder. The most common phenotypic characteristics include pre‐ and… Expand
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2013
2013
We report on a pedigree with a pair of brothers each with minor anomalies, developmental delay, and autistic‐symptoms who share… Expand
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2009
2009
We report on the analyses of four unrelated patients with de novo, overlapping, hemizygous deletions of the long arm of… Expand
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2009
2009
Background: Recent studies have identified chromosomal regions linked to variation in high density lipoprotein cholesterol (HDL-C… Expand
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Highly Cited
2006
Highly Cited
2006
Identification of genetic copy number changes in glial tumors is of importance in the context of improved/refined diagnostic… Expand
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Review
2005
Review
2005
  • J. Loughlin
  • Expert reviews in molecular medicine
  • 2005
  • Corpus ID: 24307174
Osteoarthritis (OA) is a common disease characterised by the degeneration of the cartilage of synovial joints such as the hip and… Expand
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2004
2004
The origin of the small extra chromosome in the cat eye syndrome (CES) has been repeatedly disputed (Feldman and Sparkes 1978… Expand
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1982
1982
Human phosphoglycerate mutase (PGAM, EC 2.7.5.3) is under the control of two structural loci that code for subunits A and B. By… Expand
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