The probability that the daughter is a heterozygote for both genes is 1.0
What is achondroplasia dwarfism?
The fibroblast growth factor receptor is a protein in the body that is impacted by the genetic disorder achondroplasia. This protein starts to behave incorrectly in a condition called achondroplasia, which slows the formation of bone in the growth plate cartilage.
As achondroplasia dwarfism is an autosomal dominant disorder it will be passed on to the daughter.
What is red-green color blindness?
The most prevalent form of color blindness is red-green color blindness. This disorder, also known as deuteranopia, is most likely a congenital one. In this, the person is unable to distinguish between red and green colors.
As this disease is X-linked and the mother is affected hence it will be transmitted to her daughter.
Hence, the daughter will carry the genes for both diseases and thus will be heterozygote.
To learn more about X-linked disease visit the link:
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It is not possible to see the different phases of mitosis in plant cells under a low-power objective microscope.
Under low-power objectives, individual plant cells can be seen as room-like compartments but the essential details of the contents of the cells cannot be seen. Thus, all the cells appear the same as if they are in an interphase phase of the cell cycle.
In order to view the different phases of mitosis in plant cells, higher magnifications such as high power would be required.
More on microscope magnification can be found here: brainly.com/question/20218099
Mutuaism
because they both benift from each other
Answer:
D.
Explanation:
The dominant genotype is tall, which is the capital T and the non dominant (short) is t. Because all of them have the tall dominant gene, all of them will be tall, but half of them have the heterozygous gene with both the tall and short gene, meaning they can pass it off to their offspring, but they temselves are tall.
If a mutation occurs in the genes of reproductive cells (gametes) that mutation is termed a germinal mutation. <span>Germinal mutations usually are not expressed in the individual containing the mutation, but gametes that carry the mutation will pass it on to the offspring. So, we say that the germinal mutations are hereditary mutations, inherited from a parent and present in every somatic and germline cell in the offspring.</span>