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Kindly review my answers on the genotypes part. Please give me the correct answers if incorrect. Thank you.
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- Given the pedigree below, answer the questions that follow:Consider the selfed offspring of a AaBbCcDd individual: What is the probability that offspring will have the following genotypes: AABBCCDD AaBbCCDd ● • A_B_C_D_ BbCCDd ● ● ● ● ● 1/4 x 1/4 x 1/4 x 1/4= 1/256 1/2 x 1/2 x 1/4 x 1/2= 1/32 3/4 x 3/4 x 3/4 x 3/4= 81/256 1 x 1/2 x 1/4 x 1/2= 1/16 Same genotype as the parent? A.1 B. 1/1/12 C. D.1/8 E.1/16In this pedigree chart, what is the genotype of individual III-1? (It's circled in blue.)
- A man with Type AB blood is married to a woman with Type O blood. They have 2 natural children and one adopted child. Their blood types are shown below: Jane-A Bobby - B Gracie O Which child is adopted? Complete the Punnett Square below and answer the questions that follow. List the possible genotypes: List the possible phenotypes Who is the adopted child? Explain your answer using the information from the Punnett square.I * 1 1 I 2 1 13 1 14 1 16r 1 11171 Using the pedigree you have constructed, complete the following Punnett square using A/a. 1) Show the cross between Baila and her non-albino husband if he had no Mother's Alleles albinism in his family history: Mother's genotype: Father's genotype: Genotype %: Phenotype %: o add speaker notes Father's AllelesClassify the pedigrees by the appropriate type of sex-related inheritance. RR XY X RR RR I 30 4 5 II II 30 II 30 5 4 50 Rr Rr Rr X*Y X*XXY Rr Rr Rr Rr Rr Rr Rr III-s Ond Rr Rr T RR Rr II III III O1o 120 Rr Rr m RR Rr r XX XY XY XX r Rr Rr rr Rr Pedigree 1 Pedigree 2 Pedigree 3 Pedigree 4 Sex-linked Sex-influenced Sex-limited 07:15 15°C dO ENG 2021/11/01 HUAWEI P30 lite TRIPLE CAMERA prt sc home end insert delete F8 F9 F10 F11 F12
- A typical pedigree for a family that carries neurofibromatosis is shown below. Note that carriers are not indicated with half-colored shapes in this chart. Use the letter "N" to indicate the dominant neurofibromatosis allele, and the letter "n" for the normal allele. Use the below pedigree chart and your knowledge on how to interpret a pedigree chart to answer questions # 7-9. 1 Nn nn nn 3 nn 7. Is individual #1 most likely homozygous dominant or heterozygous? Explain how you can tell. 8. What is the genotype of individual #2? Explain how you can tell. 9. What is the genotype of individual #3? Explain how you can tell. 2)Complete each of the following statements or questions as directed: 1. In the case of inheritance of capsule shape in shepherd's purse, what was the phenotype ratio of the F2 progeny? Use the format #:# or #:#:# or #:#:#:#. 2. What genetic phenomenon is demonstrated by the results of this cross (2 words):In this case a family history revealed a genetic basis for the disorder. The pedigree is shown in Fig. 1 Below. Key Ø Female: affected Female: unaffected || IV V 5600 orize 077808 15 10 9 10 CHO વ Male: affected Male: unaffected Deceased Disease status not given Dizygotic twins Monozygotic twins Fig. 1 Disease pedigree. Five generations I, II, III, IV, V are shown. Females are represented by circles, males by squares, dizygotic (non-identical) twins by diagonal lines originating from the same point, Monozygotic (identical) twins by diagonal lines originating from the same point and joined symbols and deceased by a diagonal line through the symbol. Filled symbols indicate that the individual displays the disease phenotype. Unfilled symbols indicate that the individual does not display the disease phenotype. Carriers of the disease are not indicated. Information on disease status is not known for generation I and is omitted for the individuals represented by a symbol with an asterisk.…
- Answer the following questions given the pedigree below. Please assume that no other mutations are occurring, complete penetrance, and that the individual marked with an asterisk (*) doesn’t carry the allele causing the affected phenotype. Q4) Assuming II-2 and II-3 want to have another child. what are all the possible genotypes, and what is the percentage that their child will be affected?Assume that there is complete dominance and complete penetrance at each locus and that epistasis does not occur. (These are the same conditions we used in class). Write your answers in numeric form (not in words). Referring to the cross: Dd EE GG hh xMxm x Dd ee Gg HH xMY How many different gametes are produced by the individual of genotype DdEEGGhhXMXm? What is the probability that the first offspring from this cross will be genotype DDEeGgHhXMxm? our answer rounded properly to 5 decimal digits. What is the probability that the first offspring from this cross will be a son that shows the dominant phenotype for all loci? (Type in your answer rounded properly to 5 decimal digits.)Use the following parents to create a Punnet Square and answer the question. Cross a heterozygous father with a heterozygous mother. (You can use the legend A = normal pigmentation and a = albinism) What will be the phenotypic ratio of the children?