interpret using the punnett square below to both sets of parents (Parents A , Parents B, & Parents C).based on your results of filling in the boxes. What are the chances Parents A, Parents B, and Parents C will have a child with Sickle Cell? What are the chances the child will be a carrier for Sickle Cell?
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interpret using the punnett square below to both sets of parents (Parents A , Parents B, & Parents C).based on your results of filling in the boxes. What are the chances Parents A, Parents B, and Parents C will have a child with Sickle Cell? What are the chances the child will be a carrier for Sickle Cell?
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- Phenotype: A2B 1. Give the possible genotype/s of A:B 2. If you were to perform the blood typing of this individual, what are the expected results given the following reagents Phenotype Forward typing (reagents) Reverse typing (reagents) Anti-A Anti-B Anti-H A cells B cells Al Write "+" for presence of agglutination and "-" for absence of agglutination 3. Explain the results of the blood typing, why would there be a "+" or a "" reaction during the testing. Relate your answer to the presence/absence of antigens and/or antibodiesDiscuss two ways to prevent getting an STI.?Discuss. the.differences between."Mendelion înhertonce ys. Extensions of Mendellon nhentance. and " Mendelion: mheitence vs Non-mendelion inhentonce:
- 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?hi, can I please get help on a case study on nueroanatomy I have been struggling for a couple of hours now and can't seem to understand the study to answer the following questions. is there any way or format that i can get help. I would really appreciate it. thanks! 1. Based on the information in the case, what is the most likely neuroanatomic location for a single lesion that can explain all of the patient’s symptoms and signs? In your own words, explain how you arrived at that localization. 2.What are some possibilities for the nature of the lesion (e.g., stroke, tumor, trauma, etc.)? In your own words, explain your rationale for these options. 3. How does the laboratory data and neuroimaging demonstrate the actual lesion for the patient? Describe how you interpret the data in your own words. 4.How was the patient was treated, and how did they subsequently fare? Describe the treatment plan in your own words.Retinoblastoma: The Hits Just Keep Coming Part IV – Time to Reconvene Question Since Julie is indeed a carrier of the mutated RB1 allele and Chris is homozygous for the wild-type allele, what is the likelihood that their next child will inherit Julie’s RB1 mutation? Part V – A Different Kind of Hit Question Chris does not have an RB1 mutation, and is therefore homozygous wild-type. Julie is heterozygous for the mutation. However, Kay has inherited a different RB1 mutation than the one her mother carries. Therefore, Kay did not receive her mother’s mutant allele. Assuming that Chris really is the father, what other explanation might there be for how she got a germline mutation?
- Can you make a Genogram about the given scenario? A patient with episodic shortness of breath. The patient's father died at the age of 56 of a heart attack caused by coronary artery disease. Her mother died of colon cancer at the age of 77. Her brother died at the age of 49 of an unknown cancer, and her sister died at the age of 68 of acute renal failure caused by diabetes mellitus. The patient has four children, all of them are still alive and well.Rewrite the following sentences after correction. (03 marks) If one parent has sickle cell anemia and other has carrier genotype than there is 25 % chance that any offspring is carrier.A research team interested in mapping human genes discovered a new restriction length polymorphism (RFLP). a. First, they test the RFLP in a family with the pedigree below. The individuals colored blue are affected by hemophelia, a blood clotting disease. Dad Mom daughter1 daughter2 son1 son1 On what chromosome is the RFLP found? Explain your answer. b. Next, they genotyped (determined the RFLP polymorphism, type 1 or type 2) of daughterl's family with the results shown below: husband daughter1 %3D Are the RFLP and the hemophilia gene linked? Explain your reasoning.
- b. The following diagram shows a family tree of individuals with haemophilia. B i. Based on an X-linked recessive pattern of inheritance, work out the likely genotypes of the individuals indicated by the letters. Individual A Individual B Individual C GENOTYPE ii. If individual C has children with a normal male, what are the chances that they will have haemophilia? Explain your answer fully. iii. If individual C has children with a normal male, what are the chances that their daughters will be carriers of the condition? Explain your answer fully.reference text Ph.D Fernando, Harvard Professor of Genetic Epidemiology, knows a thing or two about Twins. He must know as he is head of the Twin Research Department where he works with about 3,500 pairs of identical twins, researching the influence of a person's genes on everything from the probability of being obese, whether or not they have religious beliefs, and, how, do they fall into sentimental issues. Anyone who is a twin, or who has ever met a pair of identical twins, can attest to how remarkably similar they are to each other, even in the rare cases of adopted twins raised in separate homes.A recent article begins with an introduction to two middle-aged twin sisters called Susan and Polly, one of the pairs of twins in the study group of the Department of Research of Harvard. Although they were treated almost as a single person growing up, with cuts from identical hair and clothes, the twins began to diverge in their teens as they they gained the freedom to make their own…Define the term Agglutination.