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15q26.3

A chromosome band present on 15q
National Institutes of Health

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15qChromosomesHSP90B2P wt AlleleIL16 wt Allele

Papers overview

Semantic Scholar uses AI to extract papers important to this topic.
Review
2015
Review
2015
Chromosomal Imbalances in Patients with Congenital Cardiac Defects: A Meta-analysis Reveals Novel Potential Critical Regions Involved in Heart Development.
OBJECTIVE Congenital cardiac defects represent the most common group of birth defects, affecting an estimated six per 1000 births… 
2015
2015
Aggressive congenital juvenile myelomonocytic leukemia associated with somatic KRAS p.G13D mutation and concurrent germline IGF1R duplication
Juvenile myelomonocytic leukemia (JMML) is a rare myeloproliferative neoplasm (MPN) of childhood with an estimated frequency of 1… 
Review
2014
Review
2014
Nonmosaic tetrasomy 15q25.2 → qter identified with SNP microarray in a patient with characteristic facial appearance and review of the literature.
2014
2014
Novel splice-site and missense mutations in the ALDH1A3 gene underlying autosomal recessive anophthalmia/microphthalmia
Aim This study aimed to identify the underlying genetic defect responsible for anophthalmia/microphthalmia. Methods In total, two… 
2010
2010
Frequent deletion of CDKN2A and recurrent coamplification of KIT, PDGFRA, and KDR in fibrosarcoma of bone—An array comparative genomic hybridization study
Very little is known about the genetics of fibrosarcoma (FS) of bone. We applied array comparative genomic hybridization (CGH) to… 
Review
2008
Review
2008
Characterization of a cryptic 3.3 Mb deletion in a patient with a “balanced t(15;22) translocation” using high density oligo array CGH and gene expression arrays
Patients with an apparently balanced translocation and an abnormal phenotype may carry a cryptic deletion/duplication at their… 
2007
2007
Molecular characterization of a ring chromosome 15 in a fetus with intra uterine growth retardation and diaphragmatic hernia
To improve the phenotype‐genotype correlation in terminal 15q deletions and ring chromosome 15 syndrome. 
2004
2004
Inverted duplication of 15q with terminal deletion in a multiple malformed newborn with intrauterine growth failure and lethal phenotype.
We describe the cytogenetic and molecular characterization of an inverted duplication of chromosome 15q with evidence of a… 
1999
1999
Assignment of human interleukin 16 (IL16) to chromosome 15q26.3 by radiation hybrid mapping.
Highly Cited
1993
Highly Cited
1993
Ring chromosome 15 involving deletion of the insulin-like growth factor 1 receptor gene in a patient with features of Silver-Russell syndrome.
An 11-year-old girl with de novo r(15) (p12q26.3) with a clinical diagnosis of Silver-Russell syndrome (SRS) is presented. She… 
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