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7p22.2

A chromosome band present on 7p
National Institutes of Health

Papers overview

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2019
2019
Turner syndrome (TS) is a congenital disease caused by complete or partial loss of one X chromosome. Low bone mineral status is a… Expand
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2017
2017
Coronary artery disease (CAD) is the leading cause of death, and genetic factors contribute significantly to risk of CAD. This… Expand
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2015
2015
Recent studies have reported that regions of homozygosity (ROH) in the genome are detectable in outbred populations and can be… Expand
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2015
2015
We report a 14-year-old Hispanic male with a microduplication of the chromosome 7p22.2 band detected through microarray analysis… Expand
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2015
2015
The identification of chromosomal breakpoints in association with human abnormal phenotypes can enable elucidation of gene… Expand
2014
2014
Worldwide, the highest prevalence of esophageal cancer (EC) occurs in Northern China. High-density SNP arrays allow… Expand
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Highly Cited
2013
Highly Cited
2013
Asbestos exposure is the main risk factor for malignant pleural mesothelioma (MPM), a rare aggressive tumor. Nevertheless, only 5… Expand
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2013
2013
OBJECTIVE To investigate genetic causes in Chinese women with primary ovarian insufficiency (POI) for Genome-wide copy number… Expand
2005
2005
Uterine leiomyomas are extremely common, benign, smooth muscle tumors that represent a significant public health problem… Expand
2003
2003
We report on the cytogenetic findings from a patient with a de novo TNF-receptor-associated periodic syndrome (TRAPS), who showed… Expand