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The scientific study of inheritance is called genetics.

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Disease genes never provide biological advantages for human populations,regardless of the circumstances.

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Many of the polypeptides formed by encoded genes are enzymes that control and regulate chemical reactions in the cell.

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Osteogenesis imperfecta is a dominant genetic disorder of connective tissue.

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Gregor Mendel proved that "independent units" are responsible for the inheritance of biological traits.

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One specific transcribed mRNA strand will always produce the same polypeptide.

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Pseudogenes are gene fragments that can be reassembled to form a variety of polypeptides.

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One form of gene therapy uses bacteria-like DNA plasmids to carry therapeutic genes to a cell.

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The human genome contains about 200,000 genes.

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Crossing over increases genetic variation by forming new linkage patterns.

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A strand of DNA wound around a histone is called a nucleosome.

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A mutation caused by the loss of nucleotide bases in DNA sequence is called a deletion mutation.

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Chorionic villus sampling is a newer procedure than amniocentesis.

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Cystic fibrosis commonly occurs among all ethnic groups.

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An ideogram and a pedigree show almost the same information.

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A person with heterozygous sex chromosomes is a female.

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The chromosome with the fewest number of genes is carried by about only half the population.

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Nondisjunction results in gametes that produce trisomy but not monosomy in the cells of offspring.

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Genes are segments of DNA molecules.

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For an individual to have Down syndrome,one of the gametes had to have contained 24 chromosomes.

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