Walleye like the fish? Orrr is it another term
Answer:
The answer is 25%.
Explanation:
Hemophilia is a recessive illness that is x-linked.
If the husband has normal clotting ability, that means he has the dominant gene since he has only one X chromosome.
Since there is a probability that their child will have hemophilia, this means that the woman, who has 2 X chromosomes but has normal blood clotting abilities, has one dominant and one recessive hemophilia gene.
The probability that their first child will be a male is 50% and the probability that he will have hemophilia is also 50% since he will only get the Y chromosome from the father and the mother has one dominant and one recessive.
So the probability that their first child will be a son with hemophilia is 25%.
I hope this answer helps.
Depending on the purpose for which the description is needed, there are three various levels of complexity at which the vascular architecture of the liver might be described:
- The first level, known as the conventional level, is equivalent to Couinaud's classic 8-segment scheme and serves as a common language for doctors from other disciplines to define the location of localized hepatic lesions.
- The true branching of the hepatic veins and the main portal pedicles is taken into consideration in the second, surgical level, which will be used for anatomical liver resections and transplantations. Modern surgical and radiological procedures may fully exploit this anatomy, but doing so involves acknowledging that the Couinaud scheme is oversimplified and examining the vascular architecture objectively.
- The third degree of complexity, known as the academic level, is focused on the anatomist and the requirement to provide a systematization that clarifies the apparent conflicts between anatomical literature, radiological imaging, and surgical practice.
To view more questions on Liver anatomy, refer to:
brainly.com/question/14600160
#SPJ4
They're called anastomoses
Answer:
True
Explanation:
A mutation is any alteration in the genetic sequence of the genome of a particular organism. Mutations in the germline (i.e., gametes) can pass to the next generation, thereby these mutations can increase their frequency in the population if they are beneficial or 'adaptive' for the organism in the environment in which the organism lives (in this case, an insect/bug). The mutation rate can be defined as the probability of mutations in a single gene/<em>locus</em>/organism over time. Mutation rates are highly variable and they depend on the organism/cell that suffers the mutation (e.g., prokaryotic cells are more prone to suffer mutations compared to eukaryotic cells), type of mutations (e.g., point mutations, fragment deletions, etc), type of genetic sequence (e.g., mitochondrial DNA sequences are more prone to suffer mutations compared to nuclear DNA), type of cell (multicellular organisms), stage of development, etc. Thus, the mutation rate is the frequency by which a genetic sequence changes from the wild-type to a 'mutant' variant, which is often indicated as the number of mutations <em>per</em> round of replication, <em>per</em> gamete, <em>per</em> cell division, etc. In a single gene sequence, the mutation rate can be estimated as the number of <em>de novo</em> mutations per nucleotide <em>per</em> generation. For example, in humans, the mutation rate ranges from 10⁻⁴ to 10⁻⁶ <em>per </em>gene <em>per</em> generation.