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Q: A chromosome that has been broken and rejoined in a reversal sequence has undergone?
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What parts of a chromosome specify the amino acid sequence of a protein?

the sequence of bases


Changes in a DNA sequence that affect an entire chromosome or multiple chromosomes?

The DNA sequence of an entire chromosome is affected by a nitrogen base. A mutation is any mistake or change in the DNA sequence.


Is hemophilia a result of translocation?

It can be. Basically most mutations (regardless of type; translocation, reversal, transcription, etc...) can cause hemophilia if they occur within a specific part of the genetic sequencing that codes for the production of the clotting factor proteins. This genetic sequence if found in a segment of the X chromosome.


Parts of chromosome that specify amino acid sequence in protein?

pattern of sugar


What is a complete list of nucleotide sequence in a individuals chromosome?

Human Genome.


What Is part of the DNA code on a chromosome?

Each chromosome has genes on it in the form of coded base nucleotide sequence which is part of DNA.


What is the definition of chromosome mutation?

A chromosome is an organized structure of DNA and protein that is found in cells.In biology, mutations are changes to the nucleotide sequence of the genetic material of an organism.


What is the DNA sequence of an entire chromosome affected by?

it can be deletion, duplication, inversion, and translocation


What is each one?

Each chromosome has genes on it in the form of coded base nucleotide sequence which is part of DNA.


A chromosome's gene sequence that was abcdefg before modification and abcdlmnop afterward is an example of?

translocation


Describe a gene?

A chromosome.A hereditary unit consisting of a sequence of DNA that occupies a specific location on a chromosome and determines a particular characteristic in an organism. Genes undergo mutation when their DNA sequence changes.For apex it's "A piece of a chromosome."


Why does an extra copy of one chromosome cause so much trouble?

that is still not clear, and it is one of the reasons scientist have worked so hard to learn the DNA sequence for chromosome 21. Now researchers know all of the genes on the chromosome, they can begin experiments to find the exact genes that cause problems when present in three copies.