hat happens when one nucleiotide is lost or changed from the middle of a gene? Describe to me, or name, ti ould be more harmful to the developing fetus.
Q: Can you please answer this question
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Q: What happens when one nucleiotide is lost or changed from the middle of a gene? Describe to me, or…
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- Why is 26 incorrect1. What is the phenotype of the genetic disorder? 2. How does it express itself? 3. Does it cause you to be tall? 4. Your liver to function irregularly? 5. Do you feel no pain? 6. Are you born with extra teeth? 7. Does your body odor smell like maple syrup (maple syrup urine disorder)? 8.What does it do to you?Fill in the following table:
- Fill in the following boxes:Jekyll-Hyde Afflicted Spider Curse Afflicted Jekyll-Hyde/Spider Curse I O Human 1 II 1 III 4. Jekyll-Hyde disease is characterized by transformation into an unfeeling, aggressive, alter ego at night. While the "Spider Curse" is a disease that causes affected individuals to grow extra arms and extra eyes during a full moon. The genes responsible for these diseases sort independently and both traits run in one family. Based on the above pedigree answer the following questions: What is the mode of inheritance for Jekyll-Hyde disease? (Hint: look at individuals III-1 & III-3) O a. Autosomal Dominant O b. Autosomal Recessive O c. X-Linked Dominant O d. X-linked Recessive What evidence supports your hypothesis? Give at least 2 pieces of information from the pedigree that support your answer to 3a. Answer: 2. 3. 2. 2.Is cystic fibrosis a genotypic or phenotypic change? Explain your reasoning. Edit View Insert Format Tools Table, 12pt v Paragraph BIU A 2 T?く
- Explain the following1. A couple comes to a genetic councilor concerned about their chances of having a baby with cystic fibrosis disease. The husband had a sibling die of the disease. What are the chances that he is a carrier?8. ____________________ is the reciprocal exchange of DNA between two non-sister chromatids, which resultsin the rearrangement of linked alleles.Genetics of man 1)Determine the sex of the individual/patient based on your karyotyping results attached below. 2)Specify what kind of disorder this individual/patient may have based on your karyotyping results attached below .
- PCOS (polycystic ovarian syndrome ) what's on normal gene function.A couple has had a child born with neurofibromatosis. They come to your genetic counseling office for help. After taking an extensive family history, you determine that there is no history of this disease on either side of the family. The couple wants to have another child and wants to be advised about the risks of that child having neurofibromatosis. What advice do you give them?Should he go ahead and enroll on the chance that he would receive the DNA vaccine and that it would be more effective than chemotherapy? Bruce and his parents moved to a semi-tropical region of the United States when he was about 3 years old. He loved to be outside year-round and swim, surf, snorkel, and play baseball. Bruce was fair-skinned, and in his childhood years, was sunburned quite often. In his teen years, he began using sunscreens, and although he never tanned very much, he did not have the painful sunburns of his younger years. After graduation from the local community college, Bruce wanted an outdoor job and was hired at a dive shop. He took people out to one of the local reefs to snorkel and scuba dive. He didnt give a second thought to sun exposure because he used sunscreen. His employer did not provide health insurance, so Bruce did not go for annual checkups, and tried to stay in good health. In his late 20s, Bruce was injured trying to keep a tourist from getting caught between the dive boat and the dock. He went to an internist, who treated his injury and told Bruce he was going to give him a complete physical exam. During the exam, the internist noticed a discolored patch of skin on Bruces back. She told him that she suspected Bruce had skin cancer and referred him to a dermatologist, who biopsied the patch. At a follow-up visit, Bruce was told that he had melanoma, a deadly form of skin cancer. Further testing revealed that the melanoma had spread to his liver and his lungs. The dermatologist explained that treatment options at this stage are limited. The drugs available for chemotherapy have only temporary effects, and surgery is not effective for melanoma at this stage. The dermatologist recommended that Bruce consider entering a clinical trial that was testing a DNA vaccine for melanoma treatment. These vaccines deliver DNA encoding a gene expressed by the cancer cells to the immune system. This primes the immune system to respond by producing large quantities of antibodies that destroy melanoma cells wherever they occur in the body. A clinical trial using one such DNA vaccine was being conducted at a nearby medical center, and Bruce decided to participate. At the study clinic, Bruce learned that he would be in a Phase Ill trial, comparing the DNA vaccine against the standard treatment, which is chemotherapy, and that he would be randomly assigned to receive either the DNA vaccine or the chemotherapy. He was disappointed to learn this. He thought he would be receiving the DNA vaccine.