Skip to search formSkip to main contentSkip to account menu

18q22.1

A chromosome band present on 18q.
National Institutes of Health

Related topics

Related topics

3 relations
ChromosomesTNFRSF11A wt Allelechromosome 18q

Papers overview

Semantic Scholar uses AI to extract papers important to this topic.
2019
2019
Overcoming chemoresistance
2013
2013
Recurrent pre‐existing and acquired DNA copy number alterations, including focal TERT gains, in neuroblastoma central nervous system metastases
Stage 4 neuroblastomas have a high rate of local and metastatic relapse and associated disease mortality. The central nervous… 
2012
2012
[Mapping genes related to early onset major depressive disorder in Dagestan genetic isolates].
AIM The purpose of this study was to determine the molecular epidemiology of early onset major depressive disorder (MDD) in… 
2012
2012
Unbalanced three-way chromosomal translocation leading to deletion 18q and duplication 20p.
2010
2010
A maternally inherited chromosome 18q22.1 deletion in a male with late‐presenting diaphragmatic hernia and microphthalmia–evaluation of DSEL as a candidate gene for the diaphragmatic defect
Using an Affymetrix GeneChip® Human Mapping 100K Set to study a patient with a late‐presenting, right‐sided diaphragmatic hernia… 
2007
2007
A Novel Locus for Ectodermal Dysplasia of Hairs, Nails and Teeth Type Maps to Chromosome 18q22.1–22.3
Ectodermal dysplasias (EDs) are developmental disorders affecting tissues of ectodermal origin including hair, nails, teeth and… 
2007
2007
An innocuous duplication of 11.2 Mb at 13q21 is gene poor: Sub‐bands of gene paucity and pervasive CNV characterize the chromosome anomalies
A boy with autistic spectrum disorder without dysmorphisms was found to have a chromosome duplication of part of band 13q21. His… 
2007
2007
Two Novel Deletions (Array CGH Findings) in Pigment Dispersion Syndrome
Purpose: We report the first male with pigment dispersion syndrome and a balanced translocation t(10;15)(p11.1;q11.1). Methods… 
2004
2004
First non‐mosaic case of isopseudodicentric chromosome 18 (psu idic(18)(pter → q22.1::q22.1 → pter) Is associated with multiple congenital anomalies reminiscent of trisomy 18 and 18q− syndrome
Isopseudodicentric chromosome 18 is very rare and results in a combination of partial trisomy and partial monosomy of chromosome… 
1998
1998
Beckwith-Wiedemann syndrome in a child with chromosome 18q deletion.
Molecular genetic investigation of a female infant with Beckwith-Wiedemann syndrome (BWS) showed loss of IGF2 imprinting but no… 
By clicking accept or continuing to use the site, you agree to the terms outlined in our Privacy Policy (opens in a new tab), Terms of Service (opens in a new tab), and Dataset License (opens in a new tab)