Doctor Kryskowski: The autosomal dominant mode of inheritance and symptoms found in the patients from this family indicate that they suffer from Marfan syndrome. It is an inherited disorder caused by mutations in the FBN1 gene. What is the most feasible (easiest, cheapest, most reliable) way to investigate if this is the correct diagnosis?
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- Person and blood Type Probable Genotype Possible Gametes Mrs. Simons------A + IAIA + -, IAi + Mr. Simons-------A - IAIA -, IAi - Mrs. Simple------A + IAIA + -, IAi + Mr. Simple------- B + IBIB + -, IBi + Mrs. Simpson----B - IBIB -, IBi - Mr. Simpson-----O + Ii + - Baby A-------------B - IBIB -, IBi - Baby B-------------O + Ii + - Baby C-------------AB - IAIB - I just need help for possible gametes.Briefly explain this Statement "Treatment for the genetic disorders by using gene therapy " Please answer at your own words, please (400-500 words).True or false? The most common form of Down's Syndrome results from a spontaneous, somatic, gene mutation.
- QUESTION: There is an RFLP pattern that belongs to a disease. I need to find an inheritance pattern and marker related to the disease..What the genetic disease talk about? What cause of the genetic disease?Topic: Recombinant pharmaceuticals (for the production of insulin, human growth hormone or blood clotting factors) Question Describe the molecular genetics process using proper scientific terminology. Describe the steps that are involved. How is it performed?
- What cause of the genetic disease site your sources provide links to the websites to use?Question. Rewrite the following sentences after correction. (Subject: Biotechnology) The variation in the length of tandem repeat of microsatellite DNA has serious translational affects as this is due to its coding region. Correct: If one parent has sickle cell anemia and other has carrier genotype than there is 25 % chance that any offspring is carrier. Correct: Sickled WBC block the flow of blood and Calcium as they stick together and caused by frame shift mutation. Correct: The N1303K mutation in the CFTR gene of CF patients is autosomal dominant disorder due to insertion of asparagine at 1303. Correct: If a person RBCs have B surface antigen and it will clump with antigen B such clumping indicates Blood type B. Correct: Indirect ELISA can detect polygenic gene expression. Correct:Rewrite the following sentences after correction. The variation in the length of tandem repeat of microsatellite DNA has serious translational affects as this is due to its coding region. Correct: If one parent has sickle cell anemia and other has carrier genotype than there is 25 % chance that any offspring is carrier. Correct: Sickled WBC block the flow of blood and Calcium as they stick together and caused by frame shift mutation. Correct: The N1303K mutation in the CFTR gene of CF patients is autosomal dominant disorder due to insertion of asparagine at 1303. Correct: If a person RBCs have B surface antigen and it will clump with antigen B such clumping indicates Blood type B. Correct: Indirect ELISA can detect polygenic gene expression. Correct:
- How we can treatment the Sickle cell anemia by using gene therapy? Please draw at your own hands.fueled.brightspace.com/d2l/le/enhancedSequenceViewer/3300467?url=https%3A%2F%2Ff59af8a9-95f5-419c-a486-a A rdschools.com bookmarks Drive Classes B Login Page Sign In Education and Lear... Content = 1.08 Unit Test: Gene Expression - Part 1 Which statement is most accurate? Hair is different from kidneys because the cells that make up hair and kidneys have different genes All cells have the same genes, but different genes are active in different cells. As cells and tissues differentiate, they produce new genes. All cells have the same genes, and all of a cell's genes are active at the same time. #m C $ J лае 1 2 3 4 5 & 7 8Mr. I. M. Megabucks, the wealthiest man in the world, recently died. Since his death, three women have come forward. Each woman claims to have a child by Megabucks and demands a substantial share of his estate for her child. Lawyers for the estate have insisted on DNA typing of each of the alleged heirs. Fortunately, Megabucks anticipated trouble like this before he died, and he arranged to have a sample of his blood frozen for DNA typing. The results of the typing are shown in the figure below. Your job is to analyze the data and determine whether any of the children could be Megabucks' heir. Remember that every person has two of each chromosome, one inherited from his mother and one inherited from his father. Half of every person's DNA comes from his mother, and half comes from his father, so some of the DNA bands showing in the children will come from their mothers, and the rest will come from their fathers. The question is, could that father be Megabucks? For the first child,…