chromosomal mutation
chro
ˈkroʊ
krow
mo
so
ˌsɑ:
saa
mal
məl
mēl
mu
mju:
myoo
ta
teɪ
tei
tion
ʃən
shēn
British pronunciation
/kɹˈəʊməsˌɒməl mjuːtˈeɪʃən/

Definition & Meaning of "chromosomal mutation"in English

Chromosomal mutation
01

a genetic change that can affect chromosome structure or number, leading to variations in gene expression and potential genetic disorders

chromosomal mutation definition and meaning

What is a "chromosomal mutation"?

A chromosomal mutation is a change in the structure or number of chromosomes in a cell. Chromosomes, which are made up of DNA and proteins, contain genetic information that guides an organism's growth and development. A mutation can occur when there is a change in the DNA sequence or an abnormality in the number of chromosomes. This can lead to various effects, such as genetic disorders or diseases. For example, Down syndrome is caused by an extra copy of chromosome 21. Chromosomal mutations can happen spontaneously or be caused by environmental factors.

example
Examples
Learning about my daughter 's chromosomal mutation required genetic testing and counseling.
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