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15q23

A chromosome band present on 15q
National Institutes of Health

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6 relations
15qANP32A wt AlleleCSPG4 wt AlleleChromosomes

Papers overview

Semantic Scholar uses AI to extract papers important to this topic.
2018
2018
15q23 Gain in a Neonate with a Giant Omphalocele and Multiple Co-Occurring Anomalies
Background Omphalocele is a rare congenital abdominal wall defect. It is frequently associated with genetic abnormality and other… 
2013
2013
Novel mutations in enhanced S-cone syndrome.
2008
2008
Genomic aberrations in mantle cell lymphoma detected by interphase fluorescence in situ hybridization. Incidence and clinicopathological correlations
The primary genetic alteration of mantle cell lymphoma is a t(11;14)(q13;q32). Findings of this study provide novel insights into… 
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… 
2007
2007
A Genome-Wide Linkage Scan of Insulin Level–Derived Traits
OBJECTIVE—Serum insulin levels are altered in insulin resistance and insulin deficiency, states that are associated with the… 
2007
2007
Cloning and expression of a novel human gene, Isl-2, encoded a LIM-homeodomain protein
The LIM-homeodomain (LIM-HD) proteins have a homeodomain and two N-terminal LIM domains, which consist of a conserved cysteine… 
1997
1997
The human lysyl oxidase-like gene maps between STS markers D15S215 and GHLC.GCT7C09 on chromosome 15
Abstract The lysyl oxidase-like (LOXL) gene is a new member of the lysyl oxidase family, a copper-dependent enzyme that is… 
1992
1992
The c-src tyrosine kinase (CSK) gene, a potential antioncogene, localizes to human chromosome region 15q23----q25.
We have previously reported the cloning of a novel cytoplasmic tyrosine kinase, CSK. This tyrosine kinase has been shown to… 
1985
1985
Trisomy 15q23----qter due to a de novo t(11;15)(q25;q23) and assignment of the critical segment.
A 10 10/12-year-old boy with a de novo t(11;15)(q25;q23) leading to trisomy 15q23----qter was studied. The clinical features were… 
1984
1984
Distal 15q trisomy: phenotypic comparison of nine cases in an extended family.
Nine related individuals have been identified as being trisomic for the distal part of the long arm of chromosome 15 (15q23 to… 
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