inversion
the sequence of bases
Human Genome.
Each chromosome has genes on it in the form of coded base nucleotide sequence which is part of DNA.
translocation
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."
the sequence of bases
The DNA sequence of an entire chromosome is affected by a nitrogen base. A mutation is any mistake or change in the DNA sequence.
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.
pattern of sugar
Human Genome.
Each chromosome has genes on it in the form of coded base nucleotide sequence which is part of DNA.
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.
it can be deletion, duplication, inversion, and translocation
Each chromosome has genes on it in the form of coded base nucleotide sequence which is part of DNA.
translocation
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."
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.