Exam 14: Chromosomes and Human Inheritance

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Amniocentesis is

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C

Matching.Match the cause with the disorder. a.autosomal recessive inheritance; lactose metabolism is blocked b.nondisjunction of the twenty-first chromosomal pair c.X-linked recessive inheritance d.nondisjunction of the sex chromosomes -Down syndrome

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B

A chromosome's gene sequence that was ABCDEFG before modification and ABCDCDEFG afterward is an example of

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C

Classification.Answer the following questions in reference to the five items listed below. a.12 b.23 c.24 d.46 e.47 -How many chromosomes are present in each cell of the germ cell line for a tetraploid species where its normal complement of chromosomes is 48?

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Classification.Answer the following questions in reference to the five items listed below. a.12 b.23 c.24 d.46 e.47 -How many chromosomes does each somatic cell have in a human male who has two X chromosomes?

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Classification.Answer the following questions in reference to the five items listed below. a.12 b.23 c.24 d.46 e.47 -The normal sperm cell of species X carries 11 chromosomes.Following nondisjunction in the formation of secondary spermatocytes and their subsequent fertilization of normal ova, some of the zygotes will have 21 chromosomesand the remainder will have how many chromosomes?

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A chromosome's gene sequence that was ABCDEFG before damage and ABFEDCG after is an example of

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  -An X-linked carrier is a -An X-linked carrier is a

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MATCHING Matching.Choose the most appropriate answer for each. a.3n; generally sterile b.a chromosome segment is permanently transferred to a nonhomologous chromosome c.(2n - 1); a zygote deprived of a chromosome d.a repeat of a particular DNA sequence in the same chromosome or in nonhomologous ones e.(2n + 1); three chromosomes of the same kind are present in a set of chromosomes f.a piece of the chromosome is inadvertently left out during the repair process g.inhibits microtubule assembly; used in karyotyping h.a chromosome segment that has been cut out and rejoined at the same place, but backward -trisomy

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A human X-linked gene is

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MATCHING Matching.Choose the most appropriate answer for each. a.3n; generally sterile b.a chromosome segment is permanently transferred to a nonhomologous chromosome c.(2n - 1); a zygote deprived of a chromosome d.a repeat of a particular DNA sequence in the same chromosome or in nonhomologous ones e.(2n + 1); three chromosomes of the same kind are present in a set of chromosomes f.a piece of the chromosome is inadvertently left out during the repair process g.inhibits microtubule assembly; used in karyotyping h.a chromosome segment that has been cut out and rejoined at the same place, but backward -colchicine

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MATCHING Matching.Choose the most appropriate answer for each. a.3n; generally sterile b.a chromosome segment is permanently transferred to a nonhomologous chromosome c.(2n - 1); a zygote deprived of a chromosome d.a repeat of a particular DNA sequence in the same chromosome or in nonhomologous ones e.(2n + 1); three chromosomes of the same kind are present in a set of chromosomes f.a piece of the chromosome is inadvertently left out during the repair process g.inhibits microtubule assembly; used in karyotyping h.a chromosome segment that has been cut out and rejoined at the same place, but backward -triploidy

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  -The above figure represents which of the following: -The above figure represents which of the following:

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Males tend to be affected in greater numbers by X-linked recessive genetic disorders than are females because

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Classification.Select the best disorder listed below to match the following statements. a.Galactosemia b.Turner syndrome c.Klinefelter's syndrome d.hemophilia A e.Down syndrome -Color blindness is an X-linked recessive gene.Two normal-vision parents produce a color-blind child. (a) Is this child male or female? (b) What are the genotypes of the parents? (c) What are the chances that their next child will be a color-blind daughter?

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Males that tend to be taller than average and show mild mental impairment may have

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  -The Punnett square illustration above shows that theoretically -The Punnett square illustration above shows that theoretically

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  -Achondroplasia -Achondroplasia

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Classification.Select the best disorder listed below to match the following statements. a.Galactosemia b.Turner syndrome c.Klinefelter's syndrome d.hemophilia A e.Down syndrome -This disorder is an autosomal recessive disorder.

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MATCHING Matching.Choose the most appropriate answer for each. a.3n; generally sterile b.a chromosome segment is permanently transferred to a nonhomologous chromosome c.(2n - 1); a zygote deprived of a chromosome d.a repeat of a particular DNA sequence in the same chromosome or in nonhomologous ones e.(2n + 1); three chromosomes of the same kind are present in a set of chromosomes f.a piece of the chromosome is inadvertently left out during the repair process g.inhibits microtubule assembly; used in karyotyping h.a chromosome segment that has been cut out and rejoined at the same place, but backward -deletion

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