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- Draw a punnett square for each problem. Please be careful to notice whether a trait is homozygous or heterozygous. One parent has O type blood. The other parent has heterozygous B type blood. What are all the possible blood types the children may have? Answer:____________O ____________A _____________B _____________AB In a paternity case a man is accused of having fathered a child. He denies the accusation and presents the following evidence. His blood is O. The mother’s type is AB. The child has AB blood. Could he be the father? _______yes ________noPart of the difficulty of the genetics unit is knowing what type of problem you are being asked to solve and then solving it correctly. The following problems are a mix of normal Mendelian inheritance, incomplete dominance, co-dominance, sex-linked, and dihybrid crosses. Complete each of the problems below. Show your work! It’s difficult for me to know where you are making your mistakes (and help you to correct them) if I cannot see how you completed the problem. A mother had type A blood. Her husband has type B blood. They have a child with Type O blood. Is this possible? Use the Punnett square to support your answer. Is type O possible? ______________ What other blood type(s) could their future children have? ____________________________________________As a genetic counselor, you inform Susan and John that a blood test for cystic fibrosis is available. would you recommend generic testing for Susan and John?
- Instruction - Please answer them correctly - Please answer all of them, they are connected. PEDIGREE ANALYSIS and SYMBOLOGY Examine the pedigree which has X linked Dominant inheritance of disorder. Use letter X* (asterisk denotes disorder) as genotype of the individuals which can be XX, XY, X*X*, X*X and X*Y. a. What is the genotype of IV-6? b. What is the genotype of III-6? c. What is the genotype of II-3? d. What is the genotype of III-8? e. If couple I-1 and I-2 will have a son, what is the probability of having the disorder? f. If couple III-8 and III-9 will have another child, what is the probability of having the disorder? g. Theoretically, if individual IV-3 and individual IV-5 will marry and will have a child, what is the probability of having a child without the X-linked disorder?What makes the red? What is this testing used for?d. Write the genotypes of the parents used in the testcross using the correct notation Please I really need help with this thanks
- Part of the difficulty of the genetics unit is knowing what type of problem you are being asked to solve and then solving it correctly. The following problems are a mix of normal Mendelian inheritance, incomplete dominance, co-dominance, sex-linked, and dihybrid crosses. Complete each of the problems below. Show your work! It’s difficult for me to know where you are making your mistakes (and help you to correct them) if I cannot see how you completed the problem. The genes for hemophilia, a condition that causes blood not to clot properly, are located on the X chromosome. It is a recessive disorder. A man normal for blood clotting has children with a woman who is a carrier of the condition but still clots normally. What percentage of the male offspring will have normal clotting? _______________ % What percentage of the male offspring will have hemophilia? _______________ %Can someone show me why this is correct? I will like to see the possible genotypes and phenotypes together that proves the answer.The identity of Kim's biological father is unknown, but it is thought to be either Kevin or Thomas. To determine which of the two men it is, blood typing of all the persons involved was performed. Here are the results of the blood tests, including the phenotypes and possible genotypes of each person: Rachel (mother) Type AB; genotype IA, IB Kim (child) Type A; genotype is either IA, IA (if homozygous) or IA, i (if heterozygous) Kevin (alleged father #1) Type A; genotype is either IA,IA if homozygous or IA, i if heterozygous Thomas (alleged father #2) Type O; genotype is ii There are 2 DNA bands in the "fingerprint" of each person tested: mother, child, alleged father 1, and alleged father 2. Why are there two bands for each person and not three?
- For: TURNER SYNDROME 1. Please describe the ethical considerations for genetic testing while pointing out potential ethical dilemmas of care for this population. Please provide a detailed explanation specific to the question with a reference please. ThanksCould someone please help me with this grade 11 bio dihybrid cross problem in detail and how to solve this question, using a strategy? Assume that curly hair (C) is dominant to straight hair. Albinism (P ) is recessive to normal skin pigmentation. A woman who is heterozygous for curly hair and albinism has a child. The father is homozygous dominant for curly hair and has albinism. (a) Determine the possible phenotypes for their child. (double-crossing, Puneet square)(b) Calculate the four different probabilities of a child beingboth a male and of each phenotype.(c) What is the probability that the child will expressalbinism and have curly hair like his father?Part of the difficulty of the genetics unit is knowing what type of problem you are being asked to solve and then solving it correctly. The following problems are a mix of normal Mendelian inheritance, incomplete dominance, co-dominance, sex-linked, and dihybrid crosses. Complete each of the problems below. Show your work! It’s difficult for me to know where you are making your mistakes (and help you to correct them) if I cannot see how you completed the problem. Grasshoppers are black with red stripes (R), yellow stripes (Y), or both red & yellow stripes (RY). A red-striped grasshopper is crossed with red & yellow-striped grasshopper. What type of inheritance pattern is this?__________________________________________ Genotypic ratio: _____________________________ Phenotypic ratio: ____________________________