A genetic rearrangement through loss of segments of DNA or RNA, bringing sequences which are normally separated into close proximity. This deletion may be detected using cytogenetic techniques and can also be inferred from the phenotype, indicating a deletion at one specific locus.
See also reference (FX) in Slovak
delécia chromozómová
See also reference (FX) in English
Chromosome Deletion
Links
(17) - ARTICLES
(1) - MeSH descriptor
(2) - CiBaMed
(1) - BOOKS
subject heading
openseadragon
Number of the records: 1
This site uses cookies to make them easier to browse. Learn more about
how we use cookies.
