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6q22.33

A chromosome band present on 6q
National Institutes of Health

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3 relations
ChromosomesRSPO3 wt AlleleSTL wt Allele

Papers overview

Semantic Scholar uses AI to extract papers important to this topic.
2015
2015
High-resolution 400K oligonucleotide array comparative genomic hybridization analysis of neurofibromatosis type 1-associated cutaneous neurofibromas.
2015
2015
6q22.33 microdeletion in a family with intellectual disability, variable major anomalies, and behavioral abnormalities
Interstitial deletions on the long arm of chromosome six have been described for several regions including 6q16, 6q22.1, and… 
2014
2014
Segmental uniparental isodisomy of chromosome 6 causing transient diabetes mellitus and merosin‐deficient congenital muscular dystrophy
Segmental uniparental isodisomy (iUPD) is a rare genetic event that may cause aberrant expression of imprinted genes, and… 
2012
2012
Breast cancer risk assessment with five independent genetic variants and two risk factors in Chinese women
Recently, several genome-wide association studies (GWAS) have identified novel single nucleotide polymorphisms (SNPs) associated… 
2010
2010
Low‐risk variants FGFR2, TNRC9 and LSP1 in German familial breast cancer patients
To validate common low‐risk variants predisposing for breast cancer (BC) in a large set of BRCA1/2 negative familial or… 
2009
2009
The 6q22.33 Locus and Breast Cancer Susceptibility
Recently, we identified a novel breast cancer susceptibility locus at 6q22.33 following a genome-wide association study in the… 
2009
2009
Identification of DNA copy number aberrations by array comparative genomic hybridization in patients with ruptured intracranial aneurysms
2009
2009
The 6 q 22 . 33 Locus and Breast Cancer Susceptibility
Recently, we identified a novel breast cancer susceptibility locus at 6q22.33 following a genome-wide association study in the… 
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… 
Highly Cited
2002
Highly Cited
2002
Cloning and identification of a cDNA that encodes a novel human protein with thrombospondin type I repeat domain, hPWTSR
A cDNA was isolated from the fetal brain cDNA library by high throughput cDNA sequencing. The 2390 bp cDNA with an open reading… 
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