English Deutsch Français Italiano Español Português 繁體中文 Bahasa Indonesia Tiếng Việt ภาษาไทย
All categories

3 answers

A chromosome mutation is a change that involves a part of, or an entire chromosome: examples: non-homologous translocations,
additions or deletions caused by chromosomal breakage and reattachment, inversions, nondisjunction, polyploidy, to name a few .

A gene mutation involves a change in DNA, like mis- pairing of the N-bases .This is considered a biochemical change.

There are specific genetic disorders in humans associated with either chromosome or gene mutations.

2006-11-25 08:38:11 · answer #1 · answered by ursaitaliano70 7 · 0 0

Mutation = irreversible change of DNA.

Basically, there are three types, based on the severity of the change:

Change of the number of chromosomes (trisomy, monosomy)
Change of the structure of chromosomes (translocation, deletion)
Gene mutation - where the change is on the nucleotide level.

The first two are chromosome mutations, the third is gene mutation.

2006-11-28 04:09:34 · answer #2 · answered by Krumplee 2 · 0 0

ermmm arn't they the same? because genes are what makes up chromosomes.....

2006-11-25 16:12:51 · answer #3 · answered by Ryujin 3 · 0 0

fedest.com, questions and answers