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17q24.3

A chromosome band present on 17q
National Institutes of Health

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4 relations
17qChromosomesGNA13 wt AlleleMAP2K6 wt Allele

Papers overview

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2015
2015
A genome-wide pleiotropy scan for prostate cancer risk.
Highly Cited
2013
Highly Cited
2013
Identification of a Susceptibility Locus for Severe Adolescent Idiopathic Scoliosis on Chromosome 17q24.3
Adolescent idiopathic scoliosis (AIS) is the most common spinal deformity, affecting around 2% of adolescents worldwide. Genetic… 
2013
2013
Familial Microdeletion of 17q24.3 Upstream of SOX9 Is Associated With Isolated Pierre Robin Sequence Due to Position Effect
Pierre Robin sequence (PRS) is a malformation pattern characterized by the core triad of retrognathia, glossoptosis, and cleft… 
2011
2011
Identification of a complex 17q rearrangement in a metanephric stromal tumor.
Review
2009
Review
2009
Biomarkers in prostate cancer diagnosis and prognosis: beyond prostate-specific antigen
Purpose of review To review the most recent advances in genetic testing for prostate cancer risk and of new molecular diagnostic… 
Highly Cited
2009
Highly Cited
2009
Clinical utility of five genetic variants for predicting prostate cancer risk and mortality
A recent report suggests that the combination of five single‐nucleotide polymorphisms (SNPs) at 8q24, 17q12, 17q24.3 and a family… 
Highly Cited
2008
Highly Cited
2008
Cumulative effect of five genetic variants on prostate cancer risk in multiple study populations
A strong cumulative effect of five genetic variants and family history on prostate cancer risk was recently reported in a Swedish… 
Highly Cited
2006
Highly Cited
2006
Two novel translocation breakpoints upstream of SOX9 define borders of the proximal and distal breakpoint cluster region in campomelic dysplasia
The semilethal skeletal malformation syndrome campomelic dysplasia (CD) with or without XY sex reversal is caused by mutations… 
Highly Cited
2005
Highly Cited
2005
Position effects due to chromosome breakpoints that map approximately 900 Kb upstream and approximately 1.3 Mb downstream of SOX9 in two patients with campomelic dysplasia.
Campomelic dysplasia (CD) is a semilethal skeletal malformation syndrome with or without XY sex reversal. In addition to the… 
2003
2003
Variable Expression of Campomelic Dysplasia in a Father and his 46, XY Daughter
Campomelic dysplasia (CD, MIM 114290) is characterised by widespread osseous abnormalities including bowing of the long bones… 
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