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17q21.32

A chromosome band present on 17q
National Institutes of Health

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12 relations
17qCBX1 wt AlleleCDK5RAP3 wt AlleleChromosomes

Papers overview

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2015
2015
Array CGH analysis identifies two distinct subgroups of primary angiosarcoma of bone
Molecular genetic studies on vascular tumors are rare. Recently, possible involvement of MYC and KDR has been documented in a… 
2015
2015
De novo deletion of HOXB gene cluster in a patient with failure to thrive, developmental delay, gastroesophageal reflux and bronchiectasis.
2015
2015
CNVs in neurodevelopmental disorders
Copy number variations (CNVs) consist of duplications or deletions of chromosomal regions ranging from a few hundred to more than… 
2010
2010
Abstract 3860: New ovarian cancer susceptibility loci identified
Genome-wide association analyses have identified an ovarian cancer susceptibility locus near BNC2 at 9p22.2 (OR 0.82, p 5.1 × 10… 
2008
2008
A 580 kb microdeletion in 17q21.32 associated with mental retardation, microcephaly, cleft palate, and cardiac malformation.
Highly Cited
2007
Highly Cited
2007
Gene copy number analysis in malignant pleural mesothelioma using oligonucleotide array CGH
Conventional cytogenetic analyses and comparative genomic hybridization have revealed a complex and even chaotic nature of… 
2007
2007
Identification of 2 putative critical segments of 17q gain in neuroblastoma through integrative genomics
Partial gain of chromosome arm 17q is the most frequent genetic change in neuroblastoma (NB) and constitutes the strongest… 
Highly Cited
2005
Highly Cited
2005
Functional promoter polymorphism in the TBX21 gene associated with aspirin-induced asthma
Asthma is a phenotypically heterogeneous disorder with many etiologic factors and clinical characteristics. T-bet, a Th1-specific… 
1999
1999
Mapping the papillary renal cell carcinoma gene between loci D17S787 and D17S1799 on chromosome 17q21.32.
Trisomy of chromosome 17 is associated with the development of papillary renal cell tumors (RCT). We have analyzed 37 papillary… 
1999
1999
The human platelet alphaIIb gene is not closely linked to its integrin partner beta3.
alphaIIbb3 integrin is a heterodimeric receptor facilitating platelet aggregation. Both genes are on chromosome 17q21.32… 
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