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15q21.2

A chromosome band present on 15q
National Institutes of Health

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15qChromosomesEEF1B2P1 gene

Papers overview

Semantic Scholar uses AI to extract papers important to this topic.
2020
2020
Severe Phenotype in a Patient With Homozygous 15q21.2 Microdeletion Involving BCL2L10, GNB5, and MYO5C Genes, Resembling Infantile Developmental Disorder With Cardiac Arrhythmias (IDDCA)
Homozygous and compound heterozygous mutations in GNB5 gene have been associated with a wide spectrum of clinical presentations… 
2016
2016
Leaky transporters and sphincters in Barrett's oesophagus?
2016
2016
Abstract 121: Analysis and comparison of somatic copy number alterations in gastric cardia adenocarcinoma and gastric non-cardia adenocarcinoma
Gastric adenocarcinoma is one of the most common cancer type worldwide. Anatomically it may raise from the cardia or non-cardia… 
2015
2015
Clinical and Molecular Characterization of a Patient with 15q21.2q22.2 Deletion Syndrome
We report on a 16-year-old girl with a complex phenotype, including intellectual disability, facial dysmorphisms, and obesity… 
2015
2015
Development and estradiol regulation of osteogenesis in human mesenchymal stem cells
Background: The biosynthesis of estrogens from androgens is catalyzed by aromatase P450 enzyme, coded by the CYP19A1 gene on… 
2013
2013
Integrative analysis of copy number alteration and gene expression profiling in ovarian clear cell adenocarcinoma.
2010
2010
Phenotype–genotype correlation of a patient with a “balanced” translocation 9;15 and cryptic 9q34 duplication and 15q21q25 deletion
We report on a 2‐year‐old boy with intellectual disabilities, distinctive facies, hypotonia, cardiac, and renal malformations… 
2006
2006
The role of aromatase and 17-β-hydroxysteroid dehydrogenase type 1 mRNA expression in predicting the clinical outcome of human breast cancer
SummaryIntroductionThere is substantial evidence that breast cancer tissue contains all the enzymes responsible for the local… 
1998
1998
Assignment1 of human fatty-acid-Coenzyme A ligase, very long-chain 1 gene (FACVL1) to human chromosome band 15q21.2 by fluorescence in situ hybridization
Peroxisomal abnormality of human fatty-acid-Coenzyme A ligase, very long-chain 1 (FACVL1) has been considered to be related to X… 
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