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could you plz help with part c on this problem thank you!
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- Pedigree Analysis Is a Basic Method in Human Genetics Using the pedigree provided, answer the following questions. a. Is the proband male or female? b. Is the grandfather of the proband affected? c. How many siblings does the proband have, and where is he or she in the birth order?Given the karyotype shown at right, is this a male or a female? Normal or abnormal? What would the phenotype of this individual be?A proband female with an unidentified disease seeks the advice of a genetic counselor before starting a family. Based on the following data, the counselor constructs a pedigree encompassing three generations: (1) The maternal grandfather of the proband has the disease. (2) The mother of the proband is unaffected and is the youngest of five children, the three oldest being male. (3) The proband has an affected older sister, but the youngest siblings are unaffected twins (boy and girl). (4) All the individuals who have the disease have been revealed. Duplicate the counselors feat
- 1.What are the possible genotypes of the parent gametes of the corn dihybrid cross described above? 2.What is the genotype of the F1 generation of the corn dihybrid cross described above? 3.What is the phenotype of the F1 generation of the corn dihybrid cross described above? 4.What are the possible maternal and paternal genotypes of the F1 gametes of the corn dihybrid cross described above?Given the following pedigree (note that C7C, M4C, N2X, H6C, G9X, J1C, B8X, and P2X are the names of animals): Phenylketonuria (PKU) is a disease that results from a recessive gene.Suppose that two unaffected parents produce a child with PKU. a. What is the probability that a sperm from the father will contain the PKU allele?b. What is the probability that an egg from the mother will contain the PKU allele?c. What is the probability that their next child will have PKU?d. What is the probability that their next child will be heterozygous for the PKU gene?
- Phenylketonuria (PKU) is a disease that results from a recessive gene. Suppose that two unaffected parents produce a child with PKU. a. What is the probability that a sperm from the father will contain the PKU allele? b. What is the probability that an egg from the mother will contain the PKU allele? c. What is the probability that their next child will have PKU? d. What is the probability that their next child will be heterozygous for the PKU gene?1.What is the genotype of the F1 generation of the corn monohybrid cross described above? 2.What is the phenotype of the F1 generation of the corn monohybrid cross described above? 3.What are the possible maternal and paternal genotypes of the F1 gametes of the corn monohybrid cross described above?Both karyotyping and G_banding techniques show normal chromosomal pattern, however pedigree analysis revealed abnormality of genetic origin, what are the reasons of this?
- The genotype of EB27 and EB67 are unknown. Based on pedigree, what are the most likely genotype of each individual?A young couple went to see a genetic counselor because each had a sibling with cystic fibrosis. (Cysticfibrosis is a recessive disease, and neither member ofthe couple nor any of their four parents is affected.)a. What is the probability that the female of thiscouple is a carrier?b. What are the chances that their child will havecystic fibrosis?c. What is the probability that their child will be acarrier of the cystic fibrosis disease allele?1.What are the phenotypes of the parents of the corn dihybrid cross described above? 2. What are the possible genotypes of the parent gametes of the corn dihybrid cross described above? 3.What is the phenotype of the F1 generation of the corn dihybrid cross described above?