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Hennophile Balled the royal disease" bechuselmany European royal families had members with the condition. Hemophilia is...
4. Using the pedigree illustrating the inheritance of hemophilia among members of Europe's monarchy, answer the following questions. Hemophilia is a sex-linked recessive disorder. Normal daughter XX Camer daughter EdwTO Duke of Kent Victoria Prince of Sam Coburg Normalson Son with hemophilia Queen Victoria of England (no affected descendants Emperor Free of Germany Duke of Albany King Edward VII of England Beatrice Victoria Modern English royal family Alice Alix (Alexandra Tsar Nicholas ll of Russia Irene Prince Henry of Prussia...
PROBLEM 2 Sopodne Alone ingots aldem Prince Henry Prussian Royal Family - Royal Family dostoso 2 h Felipe Victoria Juan Pablo Miguel Spanish Royal Family do do Prince Prince Peter Zara Princess Princess British Royal Family Figure 6.5 Geen A Conceptual Approach, Seth Edition 2017 W. H. Freeman and Company This pedigree traces Hemophilia B through the interrelated royal families of Europe beginning in the 1800s. Hemophilia B is an X-linked recessive trait that causes excessive bleeding and bruising due...
d. Edward VII of England is the son of Queen Victoria. The modern English monarchy is descended from Edward. According to the pedigree, Edward VII is unaffected even though his mother is a carrier. Prince William is the great-great-great grandson of Edward VII. Is it possible for Prince William and Princess Catherine to have a child affected with hemophilia? Assume Princess Catherine is not affected. Explain your answer. Evolution Connection The human tongue can only detect four flavors. The front...
Draw Queen Victoria’s Pedigree 2. Queen Victoria married her first cousin, Albert, and had several children. Of her children: (a) One son, Leopold, had hemophilia A. (b) Daughter Beatrice had a daughter, Victoria, who married King Alfonso of Spain and gave birth to 7 children: the oldest and youngest children (boys) had hemophilia A, the second child (girl) had congenital deafness, the 3rd and 5th were healthy girls, the 4th was a stillborn male and the 6th, Juan (a healthy...
Given the following genotypes: QqRRSs x QqrrSs, what is the probability of producing offspring that present only one dominant feature? Show your work. For a sex-linked disorder such as hemophilia, illustrate the punnett square and pedigree for the offspring of an affected male (X Y) and carrier female (X^AX^a). Show your work. What is the probability of having an affected daughter? What is the probability of having a normal male?
6. If you cross a woman with type A blood and a man with type B and both ha dominant and one recessive allele for blood type what are the possible genotypes of their offspring? Use the Punnett square below to help you determin etermine this. 7. Choroideremia is a disease that causes degeneration of the retina of the eye. The recessive allele that causes this condition is found on the X chromosome. Using the square below, cross a woman...
1. For each of the following blood types, list the possible genotypes: Phenotype Possible Genotypes A B AB O 2. Dr. Paul is blood type O. His father was blood type A and his mother was blood type B. What were the genotypes of his parents? What are the possible blood types and phenotypic ratios expected for a cross involving these parental genotypes? 3. In the ABO blood system in human beings, alleles A and B are codominant and both are...
question 5-52 93 Dd D) dd D) aa x aa C) human height E) DI 4.Which of these crosses will only produce heterozygous offspring? B) AA x Aa C) Aa x Aa E) Aa x aa 5. Which of the following human traits is an example of codominance? A) sickle-cell anemia D) AB blood type B) variation in eye color 6. Which of the following is true regarding an individual who has inherited one sickle-cell gene and one normal gene...
For each of these problems, be sure to justify your answer(s) by including an allele key, parental cross (genotypes), phenotypes, and the resulting Punnett square representing all possible mating of eggs and sperm. 1. Tom and his wife Julie are both carriers for cystic fibrosis, an autosomal recessive disease. What is the chance that their children will have cystic fibrosis and carriers? 2. In cattle, a dominant “Dexter” gene, combined with its recessive allele, results in abnormally short legs, while...
Question 65 (1 point) Colorblindness is a condition present in males more often than females. This inheritance is Autosomal recessive Autosomal dominant X-linked or sex-linked Pleiotropy Polygenic Question 66 (1 point) Cystic fibrosis affects lungs, digestion, sweat glands, and liver bile ducts. This is an example of O Pleiotropy Polygenic Epigenetic X-linked Question 67 (1 point) Saved MacBook Pro Q $ ) % 5 & 7 4 6 8 9 0 E R T Y U 0 Question 63 (1...