A) epistasis is an interaction between two different chromosomes, and multiple alleles affect a single gene.
B) epistasis is an interaction between two genes, and multiple alleles are variants of the same gene.
C) epistasis affects males and multiple alleles occur in females.
D) epistasis only occurs in genes that have multiple alleles.
E) in epistasis one gene masks another, but one allele cannot mask the effect of another.
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Multiple Choice
A) dominant.
B) codominant.
C) incompletely dominant.
D) homozygous dominant.
E) automatically dominant.
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Multiple Choice
A) correlating a phenotype to an observable chromosomal abnormality.
B) determining the number of crossovers between genes on different chromosomes.
C) calculating the percent recombination between two genes on the same chromosome.
D) observing the number of genes on a chromosome.
E) observing environmental factors that cause a condition.
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A) Yes, because of codominance between the IA and IB alleles.
B) No, because a man with type AB blood could not contribute an i allele.
C) Yes, because of epistasis between the I and the H genes.
D) No, because the child's genotype must be ii.
E) Cannot tell from the phenotypes.
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A) gene expression profiling.
B) genome sequencing.
C) genome-wide association studies.
D) assisted reproductive technologies.
E) genetically modified organisms.
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A) the allele is masked in heterozygotes.
B) carriers do not constitute a progeny class.
C) they do not show a 1:2:1 genotypic ratio.
D) homozygotes for the lethal allele do not appear as a progeny class.
E) homozygotes for the lethal allele pass it on to half their offspring.
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A) crosses over within the same strand.
B) is inherited from the father only.
C) is present only in cells of the nervous and muscular systems.
D) it is poorer at DNA repair.
E) is present only in females.
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A) 12
B) 37
C) 250
D) 370
E) 3,700.
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A) places in the genome where a base varies among individuals in a population.
B) places in the genome where all people have identical base sequences.
C) the types of mRNAs in a cell.
D) the proteins produced in a cell.
E) how many centromeres chromosomes have in a population.
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Multiple Choice
A) 3/4
B) 1/3
C) 2/3
D) 1/4
E) 1/2
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A) 100%.
B) 50%.
C) 25%.
D) 0%.
E) 200%.
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A) pleiotropic.
B) a phenocopy.
C) incompletely penetrant.
D) multigenic.
E) completely lethal.
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Multiple Choice
A) people have many mitochondria, so the healthy ones can substitute for the affected ones.
B) as oocytes formed, those with harmful mitochondrial mutations did not have sufficient energy to survive.
C) they are difficult to diagnose because most physicians have forgotten what mitochondria are.
D) they do not produce symptoms.
E) they are not inherited from the father.
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Multiple Choice
A) a long tongue.
B) a short tongue.
C) a tongue that changes length.
D) a tongue of intermediate length.
E) a forked tongue.
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A) cystic fibrosis
B) Duchenne muscular dystrophy
C) hemophilia
D) Leber optic atrophy
E) Marfan syndrome
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A)
B)
C)
D)
E) none of these choices
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A) variable expressivity and complete penetrance.
B) an acquired phenotype.
C) late onset and early onset.
D) genetic heterogeneity and epistasis.
E) none of the above.
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Multiple Choice
A) heterozygous.
B) heterogenic.
C) heterogametic.
D) heterosexual.
E) heterostatic.
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Multiple Choice
A) RNA is an informational molecule, and many sequences are possible for a particular gene.
B) proteins are informational molecules, and many amino acid sequences are possible.
C) a gene sequence can vary in different ways and still encode a functional protein.
D) there are many humans on the planet.
E) people have many children.
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Multiple Choice
A) pleiotropic
B) penetrant
C) lethal
D) polymorphic
E) silent
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