Skip to search formSkip to main content

2q36.1

A chromosome band present on 2q
National Institutes of Health

Related topics

Related topics

3 relations
ChromosomesEPHA4 wt AlleleFARSB wt Allele

Papers overview

Semantic Scholar uses AI to extract papers important to this topic.
2015
2015
Genome-wide association study identifies new susceptibility loci for adolescent idiopathic scoliosis in Chinese girls
Adolescent idiopathic scoliosis (AIS) is a structural deformity of the spine affecting millions of children. As a complex disease… Expand
  • figure 1
  • table 1
  • figure 2
Is this relevant?
2015
2015
ADP-ribosylation factor-like 4C (ARL4C), a novel ovarian cancer metastasis suppressor, identified by integrated genomics.
Understanding the molecular mechanisms involving the initiation, progression, and metastasis of ovarian cancer is important for… Expand
  • table 1
  • figure 1
  • table 2
  • figure 2
  • figure 3
Is this relevant?
2015
2015
A Rare Co-Segregation-Mutation in the Insulin Receptor Substrate 1 Gene in One Chinese Family with Ankylosing Spondylitis
Ankylosing spondylitis (AS; MIM 106300) is a common rheumatic disease with strong genetic components affecting approximately 0.3… Expand
  • figure 1
  • table 1
  • table 2
  • table 3
  • table 4
Is this relevant?
2014
2014
PAX3 gene deletion detected by microarray analysis in a girl with hearing loss
Deletions of the PAX3 gene have been rarely reported in the literature. Mutations of this gene are a common cause of Waardenburg… Expand
  • figure 1
  • figure 2
  • figure 3
  • figure 4
  • table 1
Is this relevant?
2012
2012
Use of germline polymorphisms in predicting concurrent chemoradiotherapy response in esophageal cancer.
PURPOSE To identify germline polymorphisms to predict concurrent chemoradiation therapy (CCRT) response in esophageal cancer… Expand
  • figure 1
  • figure 2
  • table 1
  • table 2
  • figure 4
Is this relevant?
2012
2012
A familial case with interstitial 2q36 deletion: variable phenotypic expression in full and mosaic state.
Submicroscopic chromosomal anomalies play an important role in the etiology of craniofacial malformations, including midline… Expand
  • figure 1
  • figure 2
  • figure 3
  • figure 4
  • table 1
Is this relevant?
2011
2011
Identification of new schizophrenia susceptibility loci in an ethnically homogeneous, family-based, Arab-Israeli sample.
While the use of population-based samples is a common strategy in genome-wide association studies (GWASs), family-based samples… Expand
Is this relevant?
2011
2011
[Genome-wide association study of allergic diseases in Russians of Western Siberia].
Genome-wide association studies are currently considered as one of the most powerful tools to establishing the genetic basis of… Expand
Is this relevant?
2009
2009
Association of chromosome 2q36.1–36.3 and autosomal dominant transmission in ankylosing spondylitis: results of genetic studies across generations of Han Chinese families
BACKGROUND Ankylosing spondylitis (AS) is a chronic, potentially crippling, spondyloarthropathy with strong genetic components… Expand
  • figure 1
  • figure 2
  • table 1
  • figure 3
Is this relevant?
2008
2008
Linkage to chromosome 2q36.1 in autosomal dominant Dandy-Walker malformation with occipital cephalocele and evidence for genetic heterogeneity
We previously reported a Vietnamese-American family with isolated autosomal dominant occipital cephalocele. Upon further… Expand
  • figure 2
  • figure 1
  • figure 3
  • figure 4
  • figure 6
Is this relevant?