The pedigree below shows the blood types of the Jones family. Review the pedigree and determine the genotype of individual 9. AB %231 #2 A AB #7 #10 11 #12 #13 JAJA O 00O
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- The pedigree table below shows the blood types of three generations of family members. Notice that some of the blood type phenotypes have been given to you. What is the genotype of the individuals 1-6? Give the probable genotype of all other family members. 2 AB 6. A AB E Amy Brawa SeleeeeIf the father's blood type is O and the mother's blood type is B, what are the possible blood types of their 7 children with 4 boys and 3 girls? Construct a pedigree analysis chart on the blood type of their family.Use the image below to answer the following questions. Label the genotypes for ALL the family members in the pedigree above. Remember to use XX and XY when labeling. What does it mean to be a carrier? Why does Alexis have hemophilia? Is hemophilia a sex-linked disease? What does that mean and how does this pedigree show you this?
- n the space below, use colored pencils to create a pedigree with the following information. Follow the guidelines for a pedigree when creating this one. Ray and Elaine were married in 1970. They both had normal vision. They had 2 daughters and then a son. Both daughters, Alicia and Candace, had normal vision and never had any children of their own. The son, Mike, was colorblind. The son married Beth who also had normal vision and they had 2 children of their own, first Greg then Victoria. Victoria was colorblind, but Greg was not. Colorblindness is a sex-linked recessive trait. Do not forget what shapes are male and female. Place the names and genotypes of the people under their shape. Color your individuals the following: Red- for colorblindness White-for regular vision Blue- for individuals with regular vision but are carriers Green- unknown genotypeA 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)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.
- Create a 3 generation pedigree chart for the given: Blood Type B child, Blood Type B Mother and Father,In this pedigree chart, what is the genotype of individual III-1? (It's circled in blue.)The teacher suggested that the students revise their model to represent individuals who have a heterozygous genotype and are therefore carriers for the disease. Select the FOUR individuals in the pedigree that the students know for certain are heterozygous. Generation I 1 2 Generation II 4 5 6 Generation III 8 9 10 11 Unaffected male Unaffected female Affected male Affected female DO
- A mother with blood type A has a child with blood type AB. Give all possible blood types for the father of this child. Group of answer choices O B, AB A, AB A, B, O A, B, AB, OPedigree chart *questions are on the imageA man who is homozygous for blood type B is married to a woman who is heterozygous for blood type A. Do the test cross and identify the phenotypic and genotypic ratios of their offspring.