A) 1 brown eye, thin wing veins: 1 red eye, heavy wing veins
B) 1 brown eye, heavy wing veins: 1 red eye, thin wing veins
C) 1 brown eye, thin wing veins: 2 red eye, thin wing veins: 1 red eye, heavy wing veins
D) 1 brown eye, heavy wing veins: 2 red eye, thin wing veins: 1 red eye, thin wing veins
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Multiple Choice
A) daughters
B) sons
C) both sons and daughters
D) neither sons nor daughters
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Multiple Choice
A) 1 pair of alleles.
B) the number of X chromosomes.
C) the number of Y chromosomes.
D) 1 pair of autosomes.
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Multiple Choice
A) the parental origin of the normal and deleted chromosome.
B) whether or not the region is methylated properly.
C) whether a translocation event has occurred.
D) whether a nondisjunction event has occurred.
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Multiple Choice
A) to reduce the risk of genetic disease.
B) for gene therapy.
C) to change the sex of the fetus.
D) for diagnosis of genetic disorders.
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Multiple Choice
A) Mendel.
B) Morgan.
C) Knight.
D) Sutton.
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Multiple Choice
A) double the level of expression of genes on the X chromosome.
B) increase the level of expression of genes on the X chromosome by 50%.
C) decrease the level of expression of genes on the X chromosome by 50%.
D) decrease the level of expression of genes on the X chromosome by 100%.
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Multiple Choice
A) autosomal
B) gametal
C) sex-linked
D) pleiotropic
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Multiple Choice
A) y m v w
B) y w v m
C) y m w v
D) y w m v
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Multiple Choice
A) Anonymous markers are genetic markers that do not cause a detectable phenotype, but can be detected by molecular techniques.The markers correspond to specific and unique chromosomal regions, thereby allowing for the identification and ordering of particular segments of DNA.Such information was essential to the generation of a human genetic map.
B) Anonymous markers are genetic markers that cause a detectable phenotype and can't be detected by molecular techniques.The markers correspond to specific and unique chromosomal regions, thereby allowing for the identification and ordering of particular segments of DNA.Such information was essential to the generation of a human genetic map.
C) Anonymous markers are genetic markers that do not cause a detectable phenotype, but can be detected by molecular techniques.The markers correspond to specific and unique genetic regions, thereby allowing for the identification and ordering of particular segments of the chromosome.Such information was essential to the generation of a human genetic map.
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Multiple Choice
A) amniocentesis.
B) genetic counseling.
C) chorionic villi sampling.
D) a pedigree analysis.
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Multiple Choice
A) 1:2:1
B) 1:1:1:1
C) 9:3:3:1
D) 3:1
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A) be female because each cell has two X chromosomes.
B) be male because each cell has one Y chromosome.
C) display both male and female characteristics.
D) not survive.
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Multiple Choice
A) determine whether an individual that displays a dominant phenotype is homozygous for the trait.
B) determine whether an individual that displays a dominant phenotype is heterozygous for the trait.
C) gather genotype information from phenotype information.
D) identify the chromosome on which a gene is located.
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Multiple Choice
A) bivalents
B) autosomes
C) recombinant chromosomes
D) somatic chromosomes
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Multiple Choice
A) provided the initial evidence for genetic recombination.
B) provided evidence that genes located on the same chromosome do not assort independently.
C) allowed for the establishment of the first genetic map.
D) provided evidence for the physical exchange of genetic material between homologues.
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Multiple Choice
A) 9.8 cM
B) 0.98 cM
C) 90.2 cM
D) 9.02 cM
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Multiple Choice
A) Huntington's disease is sex-linked and every human has at least one X chromosome; thus, the chances are extremely high for this allele to be maintained in the human population.
B) Huntington's disease can present symptoms so mild that they appear to lack dominant expression of the allele in some individuals; in those cases, the allele is passed on to the offspring.
C) While lethal to a parent, Huntington's disease will not be lethal to the offspring since it can skip a generation.
D) Huntington's disease presents symptoms in mid-life, after most people have already had offspring.
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Multiple Choice
A) single nucleotide polymorphisms (SNPs)
B) human genome map
C) linkage data
D) markers on the Y chromosome
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Multiple Choice
A) Males are ZW, females are ZZ, and short bristles are caused by a dominant allele on the Z chromosome.
B) Males are ZZ, females are ZW, and short bristles are caused by a recessive allele on the Z chromosome.
C) Males are ZZ, females are ZW, and short bristles are caused by a dominant allele on the W chromosome.
D) Males are ZZ, females are ZW, and short bristles are caused by a dominant allele on the Z chromosome.
Correct Answer
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