The answers is simple read it in a book
Gene duplication (or chromosomal duplication or gene amplification) is any duplication of a region of DNA that contains a gene; it may occur as an error in homologous recombination, a retrotransposition event, or duplication of an entire chromosome.
Homologous chromosomes are two sister chomatids stuck together with cohesins forming a tetrad. They have the same genes but not necissarily the same alleles, so they could carry hair color, one with brown the other with blonde. So, homologous chromosomes share the same gene.
The Official Motion Pictures of the Heavyweight Boxing Contest Between Gene Tunney and Jack Dempsey - 1927 was released on: USA: 1927
What is thediffernece between homozygous and hetrozygous? Homozygous is a gene combination involving two of the same type of allels. AA,hh) hetrozygous is a gene combination involving two different types of alleles (e.g. Hh, Rr)
Gene Wilder Gene Wilder
a gene is passed on from generations and a chromosome is just found in certain cells
gene mutation, chromosomal abberations
a gene is passed on from generations and a chromosome is just found in certain cells
Huntington's disease is caused by a gene mutation, specifically in the HTT gene on chromosome 4.
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Yes, it is caused by a mutation in the gene for the protein CFTR.
Neither. It is an extra #21 chromosome.
There are many thousands of different mutations.
A gene mutation is a permanent change in the DNA sequence that makes up a gene. Mutations range in size from a single DNA building block (DNA base) to a large segment of a chromosome. A chromosomal mutation is a mutation involving a long segment of DNA, it is a any change in the structure or arrangement of the chromosomes. These mutations can involve deletions, insertions, or inversions of sections of DNA. In some cases, deleted sections may attach to other chromosomes, disrupting both the chromosomes that loses the DNA and the one that gains it.It is also referred to as a chromosomal rearrangement The differences between Gene mutation and Chromosome mutation are ; 1- Chromosome mutations involve changes in the structure of a chromosome OR the loss or gain of a chromosome while Gene mutations involve a change in the nucleotide -base sequence of a gene on a DNA molecule. 2- Chromosomal mutations are changes in the structure or the numbers of chromosomes (a gain or loss). Gene mutations involve changes in the nucleotide sequence of the DNA molecule. 3-A gene mutation is a permanent change in the DNA sequence that makes up a gene. Mutations range in size from a single DNA building block (DNA base) to a large segment of a chromosome while a chromosomal mutation is a mutation involving a long segment of DNA, it is a any change in the structure or arrangement of the chromosomes. These mutations can involve deletions, insertions, or inversions of sections of DNA. In some cases, deleted sections may attach to other chromosomes, disrupting both the chromosomes that loses the DNA and the one that gains it.It is also referred to as a chromosomal rearrangement 4-gene mutation is just a substitute in any old random nucleotide for any old random nucleotide chromosome mutation is missing of chromosome or +1 chromosome (down's syndrome).
i] spontaneous mutation ii] induced mutation iii] germinal mutation iv] somatic mutation v] chromosomal mutation vi] gene mutation are the some of the major types of mutation......
Hungtington's disease is a dominant mutation in the gene that codes for the protein 'Huntington' It only affects a single gene, the remainder of the chromosome is unaffected and therefore it is not a chromosomal abnormality
A chromosomal mutation is a change in the structure or number of a chromosome. This can involve rearrangements, deletions, duplications, or inversions of genetic material within a chromosome. These mutations can lead to genetic disorders or affect an individual's development and health.