4. Jane's father suffers from hemophilia B and her maternal grandfather was colorblind. Her first son is colorblind. Both traits are X linked, and the genes are 40 CM apart. How likely is it that her next son will have neither hemophilia nor color blindness?
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please thoroughly explain why the asnwer is b
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- in the experiment of following chromosomal dna mvement througgh meiosis, why. do you use non-sister chromatids to demobstrate crossing over? what combinatiobns of alleles could result from a crossover between BD and bd chromosomes? Identify two ways that meiosis contributes to genetic recombination. Why is it necessary to reduce the number of chromosomes in gametes, but not in other cell?An individual is known to have a genotype Aa Bb Dd. It is also known that gene A, gene B, and gene C all assort independently of each other. Draw the chromosomes present in a diploid cell. Label the genes.I am not sure how to explain what parent the nondisjunction occurred from in example 2 part 1. Sometimes nondisjunction will occur in a parent that has normal chromosome numbers and result in an offspring that has abnormal number of chromosomes. The phenotype of the affected offspring will often allow geneticists to determine in which parent and during which division of meiosis the nondisjunction occurred. In each of the examples below, assume the parents have a normal diploid chromosome complement. EXAMPLE 1: A man with the X-linked dominant condition “brown tooth enamel” and a woman with normal tooth enamel produce a son with brown tooth enamel. Let’s call the allele for brown tooth enamel “XB” and normal tooth enamel “Xb”. In which parent did the nondisjunction occur? Explain and/or illustrate Did nondisjunction occur at meiosis I or II? Explain and/or illustrate. What sex chromosomes are in the child’s somatic cells? EXAMPLE 2: The parents in the family above produce another…
- One difference between meiosis I and meiosis Il is that Select an answer and submit. For keyboard navigation, use the up/down arrow keys to select an answer. a chromosomes line up along the equatorial plane only in meiosis I. b cell division occurs only after meiosis II. homologous chromosomes separate in meiosis I; sister chromatids C separate in meiosis II. d chromosomes move toward opposite spindle poles only in meiosis II. DNA synthesis occurs prior to meiosis I; DNA is degraded during e meiosis II.The drawings below represent four possible cells produce by meiosis in a cell pf the genotype AaBb. Examine the figures below and answer the questions that follow: 1. How many different types of cells are produced at the end of Meiosis I? A *Write your answer as a word, not a number 2. Is there any other way you could have arranged the chromosomes? For example, a. Could A and a be arranged so that both go to the same cell after Metaphase I (Yes/No)? B b. Could B and b be arranged so that both go to the same cell after Metaphase I (Yes.No)? C c. Could A and B be arranged so that both go to the same cell after Metaphase I (Yes/No)? D d. Could A and b be arranged so that both go to the same cell after Metaphase I?(Yes./No) E 3. Are the daughter cells haploid, or diploid? F 4. Do the daughter cells have the same genetic composition as the original cell (Yes/No)? G 5. Focus on the four daughter cells…The organism you are working with has the following chromosomes. Place the chromosomes of this organism onto the cell below such that the diagram accurately shows a primary meiocyte from this organism in metaphase I of meiosis. Note 1: Only place chromosomes you need. You don't need them all. Note 2: You can place the 'Blank Box' image if you don't think you need a chromosome at a particular position. Dashed linethe metaphase plate
- Each of the drawings below shows a cell and its chromosomes in schematic form. Each one illustrates a different arrangement of sister chromatid pairs on the spindle at metaphase. Imagine that these cells come from a diploid organism who is heterozygous at two loci residing on separate chromosomes: A (with alleles A and a) and B (with alleles B and b). A D A E DC ALJAaja #11 F BBbb B BB ALJA Which of these drawings illustrate a normal chromosomal arrangement at metaphase of mitosis? Choose all that apply. 24² A Aa Ja HA bbBB ANAIn an attempt to simplify meiosis for the benefit of students, mad scientists develop a way of preventing premeiotic S phase and making do with having just one division,including pairing, crossing over, and segregation. Wouldthis system work, and would the products of such a system differ from those of the present system?Hi, I'm having some trouble with this practice problem from my study guide. If anyone can explain it it would be very helpful! Sometimes nondisjunction will occur in a parent that has normal chromosome numbers and result in an offspring that has abnormal number of chromosomes. The phenotype of the affected offspring will often allow geneticists to determine in which parent and during which division of meiosis the nondisjunction occurred. In each of the examples below, assume the parents have a normal diploid chromosome complement. EXAMPLE 1: A man with the X-linked dominant condition “brown tooth enamel” and a woman with normal tooth enamel produce a son with brown tooth enamel. Let’s call the allele for brown tooth enamel “XB” and normal tooth enamel “Xb”. In which parent did the nondisjunction occur? Explain and/or illustrate Did nondisjunction occur at meiosis I or II? Explain and/or illustrate. What sex chromosomes are in the child’s somatic cells? EXAMPLE 2: The parents in the…
- Hi, I'm having some trouble with this practice problem from my study guide. If anyone can explain it it would be very helpful! Sometimes nondisjunction will occur in a parent that has normal chromosome numbers and result in an offspring that has abnormal number of chromosomes. The phenotype of the affected offspring will often allow geneticists to determine in which parent and during which division of meiosis the nondisjunction occurred. In each of the examples below, assume the parents have a normal diploid chromosome complement. A man with the X-linked dominant condition “brown tooth enamel” and a woman with normal tooth enamel produce a son with brown tooth enamel. Let’s call the allele for brown tooth enamel “XB” and normal tooth enamel “Xb”. EXAMPLE 1: The parents in the family above produce another son, this time with two Y chromosomes and normal tooth enamel. In which parent did the nondisjunction occur? Explain and/or illustrate. Did nondisjunction occur at meiosis I or II?…The gene asSociated with the recessive disorder hemophilia is on the X chromosome, where h is the recessive copy and H is the dominant copy. The picture ("starting cell") shows a diploid cell from a male who has hemophilia, showing his X and Y chromosomes. Starting cell Xh Y Which of these pictures A-E will NOT occur at any time in meiosis of this starting cell? Select ALL that apply. D Xh Xh C YIY В X YI YY E Xh Y A X Xh ¡YYYour textbook stated, "The random segregation into daughter nuclei that happens during the first division in meiosis can lead to a variety of possible genetic arrangements." Explain how this is the case; how this is true? Be specific.