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The three main parts of a chromosome are the centromere, which holds sister chromatids together, the telomeres at each end, which protect the chromosome from deteriorating, and the chromatin, which contains DNA and proteins that help organize and package the DNA.
The parts of a chromosome that control inherited traits is referred to as genes. There are many types of inherited traits, some visible while the others are invisible,
Chromatids
The two genes are located on different chromosomes and therefore cannot be considered part of the same chromosome. Each chromosome consists of a single linear double-stranded DNA molecule and may contain numerous genes.
Well, as far as I know, DNA interacts with the following cell parts: Nucleus, Chromosome, Ribosomes, & Cytoplasm.
Deletion is the loss of a segment of DNA, duplication is the replication of a DNA segment, inversion is the flipping of a DNA segment, and translocation is the movement of a DNA segment to a new location in the genome. These are all types of structural variations that can lead to genetic disorders or diversity in populations.
The three main parts of a chromosome are the centromere, which holds sister chromatids together, the telomeres at each end, which protect the chromosome from deteriorating, and the chromatin, which contains DNA and proteins that help organize and package the DNA.
The Centromere
Centromere.
The parts of a chromosome that control inherited traits is referred to as genes. There are many types of inherited traits, some visible while the others are invisible,
An exchange of chromosome segments is called a translocation. In genetics, it refers to a chromosome abnormality caused by rearrangement of parts between nonhomologous chromosomes.
chromatid
There is the xiphoid process (a small piece of cartilage at the base of your sternum)XX chromosome...orXY chromosome:)
self similarity_ APEX or Self-similarity is the quality of being made up of parts that are small copies of the whole____True
pattern of sugar
Chromatids
A chromosomal mutation is a change in the structure or number of chromosomes, such as deletions, duplications, inversions, or translocations. These mutations can lead to changes in the distribution of genes, which may result in genetic disorders or changes in an individual's characteristics.