Exam 29: Heredity

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How might carriers of deleterious genes be recognized?

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Carriers of deleterious genes may be recognized if their offspring show symptoms of the condition or disease caused by the deleterious gene.Because the genes are usually recessive,they would show phenotypically only if the offspring received the recessive genes from both parents.A pedigree analysis may be done to trace a particular trait back through several generations.Blood chemistry tests (and DNA probing)may also be done if particular genetic traits are suspected.

Match the following: -The dominant gene is expressed when present; the recessive gene is expressed only in the absence of the dominant gene.

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C

Match the following: -Means by which genes trade places,some maternal and some paternal on each chromosome.

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C

What is (are)the genotype(s)of the first-generation offspring?

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Hereditary characteristics are transmitted to offspring by genes.

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Inheritance of stature (height)in humans is probably due to ________.

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A woman has blond hair and brown eyes.This statement is best described as indicating ________.

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The cleft chin trait follows a dominant-recessive inheritance pattern with cleft chin being the dormant trait.John is heterozygous for a cleft chin as is his wife Betty.John and Betty have three kids all of which have a cleft chins.According to Punnett square prediction what is the likely hood that their next child will have a cleft chin?

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Those characteristics that can be determined on superficial inspection of an individual are known as ________.

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A patient is heterozygous for sickle-cell anemia.Explain why the patient would have few or no symptoms of sickle-cell anemia.

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Match the following: -Lack of skin pigmentation.

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Match the following: -Situation in which an individual has different alleles making up the genotype for a particular trait.

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What would the parental gametes be from a cross of two second-generation,straight-shorthaired individuals?

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An example of multiple-allele inheritance is ________.

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Two alleles expressing exactly the same information for a trait are designated as ________.

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What were the genotypes of the parental (P1)individuals?

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A chromosomal aberration in which part of a chromosome is lost is known as ________.

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The second-generation phenotypes would follow what ratio? (Pair the number with a phenotype in each case.)

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________ disease is a disorder of brain lipid metabolism and is an example of a recessive trait.

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In meiosis the spermatozoa that are produced are genetically unlike each other and unlike the cell that produces them.This is one reason for the great variation among humans.What causes this effect?

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