Sue's chromosome #18 pair looks like this: Bob's chromosome #18 pair looks like this: Bob and Sue have a stillborn son with three copies of chromosome #18 that look like this: In which parent did non-disjunction occur? O Sue Bob You need additional information to determine which parent
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- Assume that a meiotic-nondisjunction event causes trisomy 8 in a newborn. If two of the three copies of chromosome 8 are absolutely identical, at what point during meiosis did the nondisjunction event take place?A woman who sought genetic counseling is found to be heterozygousfor a chromosomal rearrangement between the second andthird chromosomes. Her chromosomes, compared to those in anormal karyotype, are diagrammed on the next page:(a) What kind of chromosomal aberration is shown?Sue's chromosome #18 pair looks like this: Bob's chromosome #18 pair looks like this: Bob and Sue have a stillborn son with three copies of chromosome #18 that look like this: In which parent did non-disjunction occur? You need additional information to determine which parent O Bob A- O Sue 모
- 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 plateThe 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 line - the metaphase plate 1.What type of nondisjunction is the chromosome abnormality? Trisomy Or Monosomy
- A diploid fruitfly has 8 chromosomes. How many chromosomes are present in an individual with trisomy in Chromosome 1 and Chromosome 2? A person is born with two X chromosomes, trisomy 21 and two copies of other chromosomes. How many chromosomes are present in this individual? * A couple is planning to have three children. What is the probability of having all boys? *A phenotypically normal individual has the following combinations of normal and abnormal chromosomes:The normal chromosomes are shown on the left in each pair.Suggest a series of events (breaks, translocations, crossovers, etc.)that may have produced this combination of chromosomes.The karyotype of a young girl who is affected with familialDown syndrome revealed a total of 46 chromosomes. Her olderbrother, however, who is phenotypically unaffected, actually had45 chromosomes. Explain how this could happen. What wouldyou expect to be the numbers of chromosomes in the parents ofthese two children?
- A woman who sought genetic counseling is found to be heterozygousfor a chromosomal rearrangement between the second andthird chromosomes. Her chromosomes, compared to those in anormal karyotype, are diagrammed on the next page:(a) What kind of chromosomal aberration is shown? (b) Using a drawing, demonstrate how these chromosomeswould pair during meiosis. Be sure to label the differentsegments of the chromosomes.(c) This woman is phenotypically normal. Does thissurprise you? Why or why not? Under what circumstancesmight you expect a phenotypic effect of such arearrangement? The woman in above problem has had two miscarriages. Shehas come to you, an established genetic counselor, with thesequestions:(a) If not, what is the chance that she could have a normalchild? Provide an informed response to her concernsA woman who sought genetic counseling is found to be heterozygousfor a chromosomal rearrangement between the second andthird chromosomes. Her chromosomes, compared to those in anormal karyotype, are diagrammed on the next page:(a) What kind of chromosomal aberration is shown? (b) Using a drawing, demonstrate how these chromosomeswould pair during meiosis. Be sure to label the differentsegments of the chromosomes.(c) This woman is phenotypically normal. Does thissurprise you? Why or why not? Under what circumstancesmight you expect a phenotypic effect of such arearrangement? The woman in above problem has had two miscarriages. Shehas come to you, an established genetic counselor, with thesequestions:(a) Is there a genetic explanation of her frequent miscarriages?are sex chromosomes the smallest chromosome in a karyogram? if not, then why are they last?