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Biology, 22.06.2019 12:00
Refer to the family pedigree shown here. in generation i, one parent is affected by the gene mutation and one parent isn't. in generation ii, all three children are affected by the gene mutation. what can you conclude about this gene mutation? a. all children born in future generations will be affected by this disorder. b. this gene mutation is a dominant disorder. c. this gene mutation is a recessive disorder. d. the generation i mother is a carrier of this gene mutation.
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Biology, 22.06.2019 20:10
18. determine whether each stateme blank space given. ach statement is true (t) or false (f). place your answer in the 8. when a cell is put into an isotonic solution, individual wat put into an isotonic solution, individual water molecules cannot move back and forth across the cell membrane. d. when a cell is put into a hypertonic solution, there is a net movement of water molecules across the cell membrane into the cell. c. when a cell is put into a hypotonic solution, there is a net movement of water molecules across the cell membrane out of the cell. d. the movement of any solvent across a semi-permeable membrane is called osmosis. e. carrier proteins have the ability to change shape and physically move molecules across the cell membrane. f. in facilitated diffusion, the concentration of the molecules to be moved across the cell membrane is higher inside the cell.
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Biology, 22.06.2019 20:50
Suppose a point mutation, such as a change from an adenine to a guanine, occurs in the genome of a human sperm cell. the mutation could occur in any region of a gene. the effect of the mutation on the phenotype of the offspring will be determined by where the mutation occurs and its effect on the final gene product. in which of the following scenarios could the mutation alter the phenotype of the offspring? select all of the scenarios that apply the mutation occurs in the promoter and affects the rate of gene transcription. the mutation results in a new, dominant allele the mutation occurs in a portion of an intron not responsible for exon splicing the mutation occurs in a gene that controls development and alters differentiation of a cell type during development. the mutation occurs in a codon and alters the function of the final protein e mutation occurs in a codon, and the amino acid sequence of the final protein is unchanged.
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