7p12.1

A chromosome band present on 7p
National Institutes of Health

Topic mentions per year

Topic mentions per year

2006-2016
012320062016

Papers overview

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2017
2017
BACKGROUND Two key issues in prostate cancer (PCa) that demand attention currently are the need for a more precise and minimally… (More)
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2016
2016
BACKGROUND Achondroplasia is a well-defined and common bone dysplasia. Genotype- and phenotype-level correlations have been found… (More)
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2014
2014
Epilepsy affects approximately 1% of the world's population. Genetic factors and acquired etiologies, as well as a range of… (More)
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2013
2013
Hirschsprung disease (HSCR, OMIM 142623) is a developmental disorder characterized by the absence of ganglion cells along… (More)
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2011
2011
We present an infant with a de novo cytogenetically visible interstitial deletion of approximately 21.9Mb involving chromosome… (More)
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Review
2010
Review
2010
Copy number losses in chromosome arm 9p are well-known aberrations in malignancies, including leukemias. The CDKN2A gene is… (More)
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2010
2008
2008
The search for target genes involved in unbalanced acquired chromosomal abnormalities has been largely unsuccessful, because the… (More)
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2007
2007
The dic(7;9)(p11 approximately 13;p11 approximately 13) is a recurrent chromosomal abnormality in acute lymphoblastic leukemia… (More)
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2006
2006
BACKGROUND Genetic mutations are the most common cause of hypertrophic cardiomyopathy (HCM) and an increasingly recognized cause… (More)
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