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10q24.32

A chromosome band present on 10q.
National Institutes of Health

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5 relations
BTRC wt AlleleChromosomesMIR146B wt AlleleNT5C2 wt Allele

Papers overview

Semantic Scholar uses AI to extract papers important to this topic.
2019
2019
[Congenital ectrodactyly caused by chromosome 10q24.31 duplication and its pathogenetic analysis].
In order to investigate the genetic variations and the clinical manifestations of a range of congenital ectrodactyly family and… 
2018
2018
A Novel PTCH1 Frameshift Mutation Leading to Nevoid Basal Cell Carcinoma Syndrome
Nevoid basal cell carcinoma syndrome (NBCCS), also known as Gorlin syndrome, is a rare multisystemic autosomal dominant disorder… 
Review
2018
Review
2018
[The current review and prospects of the genetic study and clinical treatment of adolescent idiopathic scoliosis].
  • Y. Qiu
  • Zhonghua wai ke za zhi [Chinese journal of…
  • 2018
  • Corpus ID: 52007278
This review mainly focused on the etiology and the surgical strategy for adolescent idiopathic scoliosis (AIS) treatment. Genome… 
2016
2016
Leaky transporters and sphincters in Barrett's oesophagus?
2015
2015
The Genetic Architecture of Arsenic Metabolism Efficiency:A SNP-Based Heritability Study of Bangladeshi Adults
Background Consumption of arsenic-contaminated drinking water adversely affects health. There is interindividual variation in… 
2015
2015
Arsenic metabolism phenotypes show distinct associations with sex, BMI, socioeconomic status, 10q24.32 SNPs, and arsenic exposure
2012
2012
Abstract 2925: Genome-wide association study identifies 10q24.32 variants associated with arsenic metabolism and premalignant skin lesion risk in Bangladesh
2010
2010
AMY2A: a possible tumor-suppressor gene of 1p21.1 loss in gastric carcinoma.
Homozygous deletions (HDs) are major genomic forces contributing to the development of many solid tumors. To identify critical… 
2009
2009
Abstract 1785: Two New Susceptibility Loci for Coronary Artery Disease on Chromosomes 2p24.3 and 10q24.32
2005
2005
Identification of a Novel Homozygous Deletion Region at 6q23.1 in Medulloblastomas Using High-Resolution Array Comparative Genomic Hybridization Analysis
Purpose: The aim of this study is to comprehensively characterize genome copy number aberrations in medulloblastomas using high… 
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