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7p12.1

A chromosome band present on 7p
National Institutes of Health

Papers overview

Semantic Scholar uses AI to extract papers important to this topic.
2018
2018
Eye movements are considered endophenotypes of schizophrenia. However, the genetic factors underlying eye movement are largely… Expand
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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… Expand
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2016
2016
BackgroundAchondroplasia is a well-defined and common bone dysplasia. Genotype- and phenotype-level correlations have been found… Expand
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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… Expand
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2013
2013
Hirschsprung disease (HSCR, OMIM 142623) is a developmental disorder characterized by the absence of ganglion cells along… Expand
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2011
2011
We present an infant with a de novo cytogenetically visible interstitial deletion of approximately 21.9Mb involving chromosome… Expand
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2010
2010
 
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Highly Cited
2008
Highly Cited
2008
The search for target genes involved in unbalanced acquired chromosomal abnormalities has been largely unsuccessful, because the… Expand
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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… Expand
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2006
2006
BACKGROUND Genetic mutations are the most common cause of hypertrophic cardiomyopathy (HCM) and an increasingly recognized cause… Expand
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