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3q26.3-q27

A chromosome band present on 3q
National Institutes of Health

Papers overview

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2016
2016
ABSTRACT Clinical anophthalmia is a rare inherited disease of the eye and phenotype refers to the absence of ocular tissue in the… 
2014
2014
SRY (sex determining region Y)-box 2 (SOX2), is a transcription factor that is essential for maintaining self-renewal, or… 
2012
2012
The duplication of chromosome 3q is a rare disorder with varying chromosomal breakpoints and consequently symptoms. Even rarer is… 
2008
2008
Supernumerary marker chromosomes (SMCs) lacking alpha‐satellite sequences and possessing a newly derived functional centromere… 
2006
2006
Gene amplification is one of the mechanisms to activate oncogenes in many cancers, including esophageal adenocarcinoma (EA). In… 
2005
2005
Dup(3q) syndrome is characterized by typical facial features, mental and growth retardation, often with congenital heart defects… 
1999
1999
Inherited thrombocytopenias are a heterogenous group of disorders. Different criteria have been suggested to classify the forms…