Joe has classic hemophilia, an X-linked recessive disease. Could Joe have inherited the gene for this disease from the following people? Yes No a. His mother's mother b. His mother's father c. His father's mother d. His father's father
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- If your father were diagnosed with an inherited disease that develops around the age of 50, would you want to be tested to find out whether you would develop this disease? If so, when would you want to be tested? As a teenager or sometime in your 40s? If not, would you have children?The pedigree for Queen Victoria of England, acarrier of hemophilia A, shows the transmission tosome of her descendants, including members ofmany royal families in Europe, such as Russia andSpain, but not Germany. Hemophilia A does notaffect anyone in the present British royal family.Can you explain why hemophilia A hasdisappeared from one family and appeared inothers?A mutation that occurs to a bone marrow stem cell (restocks blood cells) in an adult individual is heritable to all the cells that are descended from it but is not passed on to their future children. O True False
- A recently married man and woman discover that eachhad an uncle with alkaptonuria (black urine disease), arare disease caused by an autosomal recessive allele of asingle gene. They are about to have their first baby. Whatis the probability that their child will have alkaptonuria?/d/1n5NtidRwTwUzcDkDPi5Z9P_SHPZ91A-XH-pfftLbhNc/edit (1) O pols Add-ons Help Last edit was seconds ago BIUA ミ: 12 + ext Calibri I|1 6 I 2 Section 5: Trihybrid cross and Laws of probability For a trihybrid cross, in which inheritance of alleles for three genes is tracked, drawing a Punnett square that combines all three genes may not be practical. Instead the laws of probability may be used. The product law of probabilities says that when alleles for separate genes segregate independently, we can figure out the probability of a particular combined genotype by multiplying the probability of the alleles for each gene. 13. We cross a homozygous tall pea plant with yellow, round seeds to a homozygous dwarf pea plant with green, wrinkled seeds. All the F1 offspring are all tall plants with yellow, round seeds. a. What are the expected F2 ratios (use fractions) of tall and dwarf plants? b. What are the expected F2 ratios (use fractions) of yellow and green seeds? C. What are the expected F2…Jekyll-Hyde Afflicted Spider Curse Afflicted Jekyll-Hyde/Spider Curse I O Human 1 II 1 III 4. Jekyll-Hyde disease is characterized by transformation into an unfeeling, aggressive, alter ego at night. While the "Spider Curse" is a disease that causes affected individuals to grow extra arms and extra eyes during a full moon. The genes responsible for these diseases sort independently and both traits run in one family. Based on the above pedigree answer the following questions: What is the mode of inheritance for Jekyll-Hyde disease? (Hint: look at individuals III-1 & III-3) O a. Autosomal Dominant O b. Autosomal Recessive O c. X-Linked Dominant O d. X-linked Recessive What evidence supports your hypothesis? Give at least 2 pieces of information from the pedigree that support your answer to 3a. Answer: 2. 3. 2. 2.
- Isaac Reynolds - Genetics and H X G what is another word for genetic X + m/d/1gmCOqwX_FMMXE_R4XOB7eq1pQgl-tXFHs6zVrbFYlmk/viewer s and Heredity Vocabular... <Zoe has cystic fibrosis. Which of the following is themost likely explanation?a. Zoe probably inherited one faulty allele from herfather, who is a carrier, and one normal allelefrom her mother.b. Zoe probably inherited one faulty allele from hermother, who must also have cystic fibrosis, andone normal allele from her father.c. Zoe must have inherited faulty alleles from bothparents, both of whom must also have cysticfibrosis.d. Zoe must have inherited faulty alleles from bothparents, both of whom are carriers.Let us practice it again! Analyze the pedigree below to answer the questions that follow. Huntington's disease a disorder in which nerve cells waste away, or disintegrate, is passed down through families. certain parts of the brain Huntington's diseate llustration ereated in htps://pregenygenetion.com/ 1. What members of the family above are affected with the Huntington's disease? 2. Tnere are no carriers ior Huntungton's disease you either have it or you do not. Is Huntington's disease caused-by a dominant or recessive trait? 3. Identify the genotypes of the following individuals using the pedigree above. (homozygous dominant, homozygous recessive, heterozygous). I- 1 II -1: II -3: III - 4 : 4. How many children did individuals I-1 and I-2 have? 5. How many girls did II-1 and II-2 have? How many have Huntington's Disease? 6. How are individuals III-2 and II-4 related? I-2 and III-5?DAmy Urown Sclence Queen Victoria was the world's most famous carrier of hemophilia. Her son, Leopold, and two carrier daughters, Alice and Beatrice, spread the allele fairly widely through the royal families of Europe, Prussia and Russia. Fortunately, no modern monarchs have inherited the allele. Indicate the probable genotype of each of the people below. Remember, hemophilia is a sex-linked trait and shaded individuals have the disease. Albert Victorla Alice Leopold Beatrice Edward George V George VI Waldamar and Alexis Alfonso and Gonzala HeinreichChromosomes and Genetics Name 1. Edward and Jenna had 4 children together. They have a few "interesting" traits, shall we say! Look at the chromosome combinations that each child received and list their genotype and phenotype. Key: D= long eyelashes B = brown eyes F= freckles G = vampire teeth T= tall W = werewolf fur d = short eyelashes b = red eyes f= no freckles g = no vampire teeth t = short w = no werewolf furi). pronde. clear- cut. explenations.in differences/Similarīties, if ony, between." Extensnons of mendelren. mhentonce Vs. Non.- mendellen. nhentnce.SEE MORE QUESTIONS