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14q31.1

A chromosome band present on 14q
National Institutes of Health

Papers overview

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2014
2014
In our previous study, we identified 1241 loci with somatic copy number alterations in human hepatocellular carcinoma (HCC) using… Expand
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2012
2012
ObjectiveThe aim of this study was to identify novel genes following genomic DNA copy number changes using a genome-wide array… Expand
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2010
2010
Tourette syndrome (TS) is a frequent neuropsychiatric disorder of unknown etiology. A number of chromosomal regions have been… Expand
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2010
2010
INTRODUCTION Non-small cell lung cancer (NSCLC) is characterized by a multitude of genetic aberrations with unknown clinical… Expand
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2009
2009
The fetus was the 1096-g product of 28-week gestation in a 31-yearold, gravida 2, para 1, mother who had undergone amniocentesis… Expand
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2007
2007
A boy with autistic spectrum disorder without dysmorphisms was found to have a chromosome duplication of part of band 13q21. His… Expand
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2006
2006
Genetic alterations have been recognized as an important event in the carcinogenesis of gastric cancer (GC). We conducted high… Expand
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2002
2002
A genome-wide linkage scan was performed for genes affecting submaximal exercise cardiac output (Q) and stroke volume (SV) in the… Expand
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2000
2000
Krabbe’s disease or globoid-cell leukodystrophy is an autosomal recessive disorder caused by a mutation of the galactocerebroside… Expand
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1999
1999
The gene for maleylacetoacetate isomerase (MAAI) (EC 5.2.1.2) was the last gene in the mammalian phenylalanine/tyrosine catabolic… Expand
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