Explanation:
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Duplications involve the production of one or multiple copies of a specified region of the genetic code
Further Explanation:
All the genetic information within the eukaryotic cell is stored within the nucleus as helical DNA. This DNA is tightly condensed and wound around histones as chromosomes. To produce daughter cells during cell division, the chromosomes (total number of chromosomes (2n)) are copied before the cell splits into two daughter cells. This process is known as mitosis, and occurs in cell division and growth processes. Two new nuclei are formed, along with identical cells. These are the same as the parent cell and the chromosome number (2n) is maintained.
Conversely in meiosis, the number of chromosomes (2n) is halved through meiotic divisions, producing 4 (n) germ cells (sperm or eggs), each containing half the number of chromosomes as its parent cell. During the process of cell division, spontaneous changes within the genome can arise. These mutations are errors occur when copies of the DNA within the cell are made; mutations may range from small changes called single nucleotide polymorphisms, to large scale deletions, and additions which span multiple genes.
Duplications involve the production of one or multiple copies of a specified region of the genetic code.
Like other events, such as crossing over during mitosis and meiosis, mutations lead to increases in genetic variation. This variation refers to the genetic characteristics present within a species. Mutations are maintained within cells, as they form new traits called alleles, which may confer adaptations that increase the fitness of a species, along with ensuring survival by conferring a protective advantage.
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The twisty columns of the double helix are phosphate and sugar(deoxyribose), which are bonded by a covalent bond. Each nucleotide consists of one of each, and also a nitrogen base. The rungs are nitrogen bases, each nucleotide has one base, and one side of the ladder bonds to the other side of the ladder through hydrogen bonding of complementary base pairs. The base pairs of DNA are A-T and C-G
They help an environment because they create an ecosystem allowing animals to thrive and live a lifecycle with the resources they need.
<span>Males and females are attracted to each other in order to ensure the viability and fertility of the offspring, which is also why it is uncommon that males of one species be attracted to females of another. Members of two different species cannot mate and thus cannot produce fertile, viable offspring, unless they are part of different sub-species. But they must be part of the same species.
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The fetus can be screened for abnormalities using karyotyping and biochemical analysis using amniocentesis and chorionic villus sample.
<h3>What data can we glean from CVS and amniocentesis?</h3>
In at-risk fetuses, these tests can detect genetic illnesses such cystic fibrosis, Tay-Sachs disease, and sickle cell disease. The main benefit of CVS over amniocentesis is that it is done considerably earlier in pregnancy—at 10 to 13 weeks as opposed to 15 to 20 weeks—thus saving more time for the mother.
<h3>What can a couple learn about their growing fetus from amniocentesis and chorionic villus sampling?</h3>
Amniocentesis and chorionic villus sampling (CVS) are prenatal diagnostic techniques used to identify certain fetal genetic disorders. The likelihood of miscarriage rises with both procedures.
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