Translocation in DNA refers to a type of chromosomal abnormality where a segment of one chromosome breaks off and becomes attached to another chromosome. This can lead to alterations in the structure and function of the affected genes, which can result in various genetic disorders or cancers.
Translocations can occur spontaneously or as a result of environmental factors such as radiation or chemicals. In some cases, translocations can also be inherited from parents.
Translocations can be detected through genetic testing, and their consequences can be managed through various medical treatments such as chemotherapy or targeted therapies.
translocation in DNA
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