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6q25.3

A chromosome band present on 6q
National Institutes of Health

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4 relations
ChromosomesGTF2H5 wt AlleleSLC22A1 wt AlleleSOD2 wt Allele

Papers overview

Semantic Scholar uses AI to extract papers important to this topic.
Review
2020
Review
2020
Striking phenotypic overlap between Nicolaides-Baraitser and Coffin-Siris syndromes in monozygotic twins with ARID1B intragenic deletion.
2020
2020
The Search for Molecular Markers in a Gene-Orphan Case Study of a Pediatric Spinal Cord Pilocytic Astrocytoma
Background/Aim: We herein presented a case of pediatric spinal cord pilocytic astrocytoma diagnosed on the basis of… 
2019
2019
Clinical presentation and genetic profiles of Chinese patients with velocardiofacial syndrome in a large referral centre
Diagnosis and treatment of velocardiofacial syndrome (VCFS) with variable genotypes and phenotypes are considered to be very… 
2015
2015
Congenital hydrocephalus and hemivertebrae associated with de novo partial monosomy 6q (6q25.3→qter)
Abstract This study was conducted to describe a prenatal case of congenital hydrocephalus and hemivertebrae with a 6q terminal… 
Review
2010
Review
2010
Ophthalmologic abnormalities in a de novo terminal 6q deletion
Purpose: To correlate the clinical phenotype with the genotype of a boy with a terminal deletion of chromosome 6q and to compare… 
2009
2009
Characterization of a complex chromosome aberration in two cases of peritoneal mesothelioma arising primarily in the hernial sac
Malignant mesotheliomas of the hernial sac are uncommon and only a few cases have been diagnosed incidentally during… 
2006
2006
A locus for sacral/anorectal malformations maps to 6q25.3 in a 0.3 Mb interval region
Partial absence of the sacrum is a rare congenital defect that also occurs as an autosomal-dominant trait, whereas imperforate… 
Review
2001
Review
2001
Terminal 6q25.3 deletion and abnormal behaviour.
A 10-year-old mentally retarded boy with terminal 6q25 deletion, dysmorphism and striking abnormal behaviour is reported. The… 
2000
2000
Mapping of Target Regions of Allelic Loss in Primary Breast Cancers to 1‐cM Intervals on Genomic Contigs at 6q21 and 6q25.3
Allelic losses on the long arm of human chromosome 6 are frequently observed in cancers of the ovary, prostate, and breast. To… 
1999
1999
Syndromal obesity due to paternal duplication 6(q24.3-q27).
The likelihood of a paternally expressing imprinted gene in chromosome region 6(q23-24) has been highlighted by cases of… 
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