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15q

Known as: Chromosome 15 Distal Arm, Chromosome 15 Long Arm 
Distal (long) arm of chromosome 15
National Institutes of Health

Related topics

Related topics

31 relations
15q11-q1315q11.215q1415q15

Papers overview

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Highly Cited
2007
Highly Cited
2007
Array CGH identifies distinct DNA copy number profiles of oncogenes and tumor suppressor genes in chromosomal- and microsatellite-unstable sporadic colorectal carcinomas
DNA copy number changes represent molecular fingerprints of solid tumors and are as such relevant for better understanding of… 
2005
2005
Microarray analysis of gene/transcript expression in Angelman syndrome: deletion versus UPD.
Highly Cited
2002
Highly Cited
2002
Detection of genetic alterations in advanced prostate cancer by comparative genomic hybridization.
2001
2001
Cytogenetic characterization of six malignant peripheral nerve sheath tumors: comparison of karyotyping and comparative genomic hybridization.
Highly Cited
2001
Highly Cited
2001
Additional complexity on human chromosome 15q: identification of a set of newly recognized duplicons (LCR15) on 15q11-q13, 15q24, and 15q26.
Several cytogenetic alterations affect the distal part of the long arm of human chromosome 15, including recurrent rearrangements… 
Highly Cited
1998
Highly Cited
1998
Gain of 3q and deletion of 11q22 are frequent aberrations in mantle cell lymphoma
We used comparative genomic hybridization (CGH) to screen for DNA copy number changes in 34 specimens from 27 cases of mantle… 
Review
1997
Review
1997
Cytogenetic studies in prostate cancer: are we making progress?
1996
1996
Gains and losses of DNA sequences in malignant mesothelioma by comparative genomic hybridization.
Highly Cited
1996
Highly Cited
1996
Assignment of Genes Coding for Brown Eye Colour (BEY2) and Brown Hair Colour (HCL3) on Chromosome 15q
Brown eye colour (BEY), or total brown iris pigmentation is one of the most common phenotypes of iris colour. Data of eye colour… 
Highly Cited
1995
Highly Cited
1995
Autosomal dominant familial spastic paraplegia: tight linkage to chromosome 15q.
Autosomal dominant, uncomplicated familial spastic paraplegia (FSP) is a genetically heterogeneous disorder characterized by… 
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