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genetics exam 4

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Question
Answer
show syntenic genes  
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The physical linkage of genes on the same chromosomes   show
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show linkage group  
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Human linkage groups   show
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show genetic recombination during crossing over  
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show recombinant phenotypes  
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Cells without crossing over   show
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Cells with crossing over   show
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The likelihood of crossing over depends on what between two genes   show
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Morgan realized that linkage of autosomal genes in Drosophila could be interpreted using   show
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show the linear order and distance  
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Genetic maps can be made by   show
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show a linkage map  
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Genetic mapping is usually done by doing   show
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recombination frequency =   show
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show a three-point test-cross analysis  
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Separates the gene in the middle from the other two genes at either end   show
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What does it mean when we say genes are syntenic   show
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Which of the following statements is true A. Genes that are closer together are less likely to experience crossing over B. Genes that are further apart are less likely to experience crossing over C. Recombination frequency overestimates the distance   show
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show a high number of purple/long and red/round then purple/round and red/long  
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What is the basis behind the production of recombinant cells   show
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show 24  
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What is the purpose of doing genetic mapping   show
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Why is the maximum recombination frequency 50%   show
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Why do recombination frequencies tend to underestimate true physical distance   show
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How do you set up a testcross   show
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The order of three genes one a chromosome is A-B-C. Genes A and B are 10 cM apart and genes B and C are 20 cM apart. From a ABC/abc individual, what is the likelihood of getting a Abc gamete   show
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Differences in alleles and chromosomes, either among members of the same species or among different species   show
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variations in specific genes, can also occur in chromosome structure and number   show
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show cytogeneticists  
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show metacentric  
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show submetacentric  
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show acrocentric  
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show Telocentric  
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show karyotype  
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show G bands  
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show deletion  
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show duplication  
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show inversion  
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Two non-homologous chromosomes swap segments   show
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show nonallelic homologous recombination  
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Type of structural variation in which a DNA segment 1000 bp or larger has copy number differences in members of the same species   show
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A gene normally found in two copies in a diploid cell may be found in three or more copies   show
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Duplications can provide additional genes leading to   show
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Two or more genes derived from a common ancestral gene are   show
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Homologous genes within a single species are called   show
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show chromosomal inversion  
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The centromere is within inverted region   show
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show paracentric inversion  
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show breakpoints  
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Gene is repositioned in a way that alters expression   show
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show an inversion loop  
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Crossover within inversion loop can lead to   show
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show dicentric chromosomes  
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Chromosome with no centromere   show
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show simple translocation  
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Two nonhomologous chromosomes exchange pieces   show
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Ends of eukaryotic chromosomes that prevent translocations from occuring   show
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Lead to rearrangement of the genetic material, not a change in the amount   show
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Carriers of a balanced translocations are at risk of having offspring with significant portion of genetic material duplicated or missing   show
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show balanced  
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show unbalanced  
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Adjacent-2 segregation   show
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What causes the most effects on phenotypes   show
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show Aneuploidy  
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Variation in the number of complete sets of chromosomes (triploidy 3n, tetraploidy 4n)   show
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show polyploid  
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show Endopolyploidy  
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show sterile  
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Failure of chromosomes to segregate properly during anaphase   show
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Nondisjunction in meiosis I   show
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Nondisjunction in meiosis II   show
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All the chromosomes can undergo nondisjunction and migrate to one daughter cell   show
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The diploid cell can participate in fertilization with a normal gamete, yielding a triploid individual   show
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show chromosome loss  
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Results from interspecies crosses usually by two closely related species   show
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show mosaicism  
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show trisomy  
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