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11p14.3

A chromosome band present on 11p
National Institutes of Health

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Chromosome 11 Short ArmChromosomes

Papers overview

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2018
2018
A case report of a Malaysian with WAGR syndrome
The Wilms tumour, aniridia, genital abnormalities and mental retardation (WAGR) syndrome is a rare genetic syndrome which is… 
2015
2015
A novel acquired cryptic three-way translocation t(2;11;5)(p21.3;q13.5;q23.2) with a submicroscopic deletion at 11p14.3 in an adult with hypereosinophilic syndrome.
  • E. Kjeldsen
  • Experimental and molecular pathology (Print)
  • 2015
  • Corpus ID: 205774605
2008
2008
β-thalassemia major evolution from β-thalassemia minor is associated with paternal uniparental isodisomy of chromosome 11p15
β-thalassemia major can be caused by homozygosity or compound heterozygosity for β-globin gene mutations (HBB gene). Most cases… 
2004
2004
Characterization of human TMEM16G gene in silico.
TMEM16A, TMEM16B, TMEM16C, TMEM16D, TMEM16E, TMEM16F and TP53I5 are TMEM16 family eight-transmembrane proteins with N- and C… 
Highly Cited
1999
Highly Cited
1999
Identification of an autoimmune enteropathy-related 75-kilodalton antigen.
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