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17q24

A chromosome band present on 17q
National Institutes of Health

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17qChromosomes

Papers overview

Semantic Scholar uses AI to extract papers important to this topic.
2016
2016
SLC44A1–PRKCA fusion in papillary and rosette-forming glioneuronal tumors
2012
2012
A genome-wide linkage study of individuals with high scores on NEO personality traits
The NEO-Five-Factor Inventory divides human personality traits into five dimensions: neuroticism, extraversion, openness… 
Review
2007
Review
2007
Hypomethylation in the 11p15 telomeric imprinting domain in a patient with Silver–Russell syndrome with a CSH1 deletion (17q24) renders a functional role of this alteration unlikely
Silver–Russell syndrome (SRS) is a clinical and genetic heterogeneous malformation syndrome. Patients show intrauterine and… 
Highly Cited
2006
Highly Cited
2006
PRKCA and Multiple Sclerosis: Association in Two Independent Populations
Multiple sclerosis (MS) is a chronic disease of the central nervous system responsible for a large portion of neurological… 
Highly Cited
2004
Highly Cited
2004
A novel mutation in the Connexin 46 gene causes autosomal dominant congenital cataract with incomplete penetrance
Congenital or paediatric cataract is a phenotypically and genetically heterogeneous disorder consisting of lens opacities in… 
2004
2004
Biochemical characterization of two GALK1 mutations in patients with galactokinase deficiency
Galactokinase (GALK1) deficiency is an autosomal recessive disorder, which causes cataract formation in children not maintained… 
2002
2002
Losses in chromosomes 17, 19, and 22q in neurofibromatosis type 1 and sporadic neurofibromas: a comparative genomic hybridization analysis.
1999
1999
Structure, alternative splicing, and expression of the human RGS9 gene.
Highly Cited
1995
Highly Cited
1995
A progressive early onset cataract gene maps to human chromosome 17q24
Cerulean cataract is an autosomal dominant, early onset, progressive cataract characterized by blue or white opacifications in… 
Highly Cited
1995
Highly Cited
1995
Autosomal dominant zonular cataract with sutural opacities localized to chromosome 17q11-12.
Congenital cataracts constitute a morphologically and genetically heterogeneous group of diseases that are a major cause of… 
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