64. A couple learned their child has a genetic disorder where a piece of a chromosome moved to another chromosome; this type of mutation is A. Duplication B. Deletion C. Inversion 65. Which of the following is an example of a frameshift mutation of the following sentence “THE FAT CAT ATE THE RED RAT"? A. THE FAT RAT ATE THE RED CAT B. THE CAT ATE THE RED RAT 66. Which of the following is not sex-linked recessive? A. Hemophilia B. Duchenne muscular dystrophy A. B. Galactosemia D. Translocation E. Nondisjunction 67. Which of the following is a dominant genetic disorder? A. Marfan Syndrome B. Hunter Syndrome 68. Which of the following is a mitochondrial genetic disorder? A. Tay Sacs B. Kearns Sayre Syndrome 69. Which of the following is a metabolic genetic disorder involved with the inability to break down Phe? Adrenoleukodystrophy C. Alkaptonuria D. Phenylketonuria 70. A human female with only one X chromosome is said to have a condition called A. X chromosome inactivation C. Turner syndrome D. Klinefelter syndrome A. Hydrophilic B. Hydrophobic C. THE FAC ATA TET HER EDR AT D. THE FAT CAT ATT THE RED RAT I C. Huntington Syndrome D. Adrenoleukodystrophy C. Tay Sacs D. Kearns Sayre Syndrome B. Jacob's syndrome 71. Sickle cell anemia is caused by a missense point mutation that changed the acidic amino acid into an amino acid that is C. Hypercholesterolemia D. Sickle cell anemia C. Acidic D. Basic
64. A couple learned their child has a genetic disorder where a piece of a chromosome moved to another chromosome; this type of mutation is A. Duplication B. Deletion C. Inversion 65. Which of the following is an example of a frameshift mutation of the following sentence “THE FAT CAT ATE THE RED RAT"? A. THE FAT RAT ATE THE RED CAT B. THE CAT ATE THE RED RAT 66. Which of the following is not sex-linked recessive? A. Hemophilia B. Duchenne muscular dystrophy A. B. Galactosemia D. Translocation E. Nondisjunction 67. Which of the following is a dominant genetic disorder? A. Marfan Syndrome B. Hunter Syndrome 68. Which of the following is a mitochondrial genetic disorder? A. Tay Sacs B. Kearns Sayre Syndrome 69. Which of the following is a metabolic genetic disorder involved with the inability to break down Phe? Adrenoleukodystrophy C. Alkaptonuria D. Phenylketonuria 70. A human female with only one X chromosome is said to have a condition called A. X chromosome inactivation C. Turner syndrome D. Klinefelter syndrome A. Hydrophilic B. Hydrophobic C. THE FAC ATA TET HER EDR AT D. THE FAT CAT ATT THE RED RAT I C. Huntington Syndrome D. Adrenoleukodystrophy C. Tay Sacs D. Kearns Sayre Syndrome B. Jacob's syndrome 71. Sickle cell anemia is caused by a missense point mutation that changed the acidic amino acid into an amino acid that is C. Hypercholesterolemia D. Sickle cell anemia C. Acidic D. Basic
Human Anatomy & Physiology (11th Edition)
11th Edition
ISBN:9780134580999
Author:Elaine N. Marieb, Katja N. Hoehn
Publisher:Elaine N. Marieb, Katja N. Hoehn
Chapter1: The Human Body: An Orientation
Section: Chapter Questions
Problem 1RQ: The correct sequence of levels forming the structural hierarchy is A. (a) organ, organ system,...
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