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7p22.2

A chromosome band present on 7p
National Institutes of Health

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3 relations
Chromosome 7 Short ArmChromosomesPAPOLB wt Allele

Papers overview

Semantic Scholar uses AI to extract papers important to this topic.
2020
2020
Cross-Cancer Genome-Wide Association Study of Endometrial Cancer and Epithelial Ovarian Cancer Identifies Genetic Risk Regions Associated with Risk of Both Cancers
Background: Accumulating evidence suggests a relationship between endometrial cancer and ovarian cancer. Independent genome-wide… 
2018
2018
Rare copy number variants in the genome of Chinese female children and adolescents with Turner syndrome
Turner syndrome (TS) is a congenital disease caused by complete or partial loss of one X chromosome. Low bone mineral status is a… 
2017
2017
Genome-Wide Linkage Analysis of Large Multiple Multigenerational Families Identifies Novel Genetic Loci for Coronary Artery Disease
Coronary artery disease (CAD) is the leading cause of death, and genetic factors contribute significantly to risk of CAD. This… 
2015
2015
A Case of the 7p22.2 Microduplication: Refinement of the Critical Chromosome Region for 7p22 Duplication Syndrome
Abstract We report a 14-year-old Hispanic male with a microduplication of the chromosome 7p22.2 band detected through microarray… 
2015
2015
Genome-wide homozygosity signature and risk of Hodgkin lymphoma
Recent studies have reported that regions of homozygosity (ROH) in the genome are detectable in outbred populations and can be… 
2015
2015
Co‐segregation of Freiberg's infraction with a familial translocation t(5;7)(p13.3;p22.2) ascertained by a child with cri du chat syndrome and brachydactyly type A1B
The identification of chromosomal breakpoints in association with human abnormal phenotypes can enable elucidation of gene… 
2013
2013
[Genome-wide copy number scan in Chinese patients with premature ovarian failure].
OBJECTIVE To investigate genetic causes in Chinese women with primary ovarian insufficiency (POI) for Genome-wide copy number… 
2011
2011
Genetic and epidemiological studies of Infantile Hypertrophic Pyloric Stenosis
Infantile Hypertrophic Pyloric Stenosis (IHPS) is a condition of early infancy characterized by thickening of the pyloric muscle… 
2005
2005
Microallelotyping defines novel regions of loss of heterozygosity in uterine leiomyomas
Uterine leiomyomas are extremely common, benign, smooth muscle tumors that represent a significant public health problem… 
2003
2003
Complex chromosomal rearrangements in a secondary acute myeloblastic leukemia after chemotherapy in TRAPS.
We report on the cytogenetic findings from a patient with a de novo TNF-receptor-associated periodic syndrome (TRAPS), who showed… 
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