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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
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2014
2014
Worldwide, the highest prevalence of esophageal cancer (EC) occurs in Northern China. High-density SNP arrays allow… Expand
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2013
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
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2005
2005
Uterine leiomyomas are extremely common, benign, smooth muscle tumors that represent a significant public health problem… Expand
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2003
2003
We report on the cytogenetic findings from a patient with a de novo TNF-receptor-associated periodic syndrome (TRAPS), who showed… Expand
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