Exam 24: Genetics and Genomics

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Identical alleles are said to be

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Freckles are a phenotype and the allele combination that causes a clotting disorder is a genotype.

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Phenylketonuria (PKU)is a genetic disease caused by mutation of the PAH gene, which normally produces the enzyme phenylalanine hydroxase. This enzyme is essential for the conversion of the amino acid phenylalanine into tyrosine. Without the enzyme, phenylalanine builds up in the blood and tissues of various body regions. It can produce severe skin discolorations and foul odor, but also intellectual disabilities and behavioral problems. Some people may experience only one type of PKU symptoms and not the others. PKU is an example of

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In a certain species of fly, eye color is designated by the W+ and w alleles, with the W+ allele being dominant. Typical eye color is red for these flies, while a rarer white color variant exists. In this species, W+ is the ________ and w is a ________.

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The approximate number of protein-encoding genes on the Y chromosome is

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The muscle disorder myotonic dystrophy can be caused by different genes, on different chromosomes. This means that the condition is genetically heterogeneic.

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Genetics is the study of

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An individual who is homozygous dominant for a trait can be symbolized

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Genetics is the study of the inheritance of traits and their variability.

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A bell curve is characteristic of the distribution of phenotypes of a multifactorial trait because

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Which of the following chromosomal abnormalities most severely affect a fetus?

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An allele that masks the effect of another is

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A recessive allele masks the effect of a dominant allele.

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A woman insists on an ultrasound and a maternal serum marker test to check for Trisomy 21 in her unborn child because she only wants to use non-invasive methods. Her obstetrician will

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Hemophilia A is

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Genetic information passes from protein to RNA to DNA.

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Gender determination for males reflects expression of

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The human genome consists of

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A human cell with 46 chromosomes is

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Cells from a woman with Turner syndrome have

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