Exam 4: Pedigree Analysis in Human Genetics
Exam 1: A Perspective on Human Genetics31 Questions
Exam 2: Cells and Cell Division54 Questions
Exam 3: Transmission of Genes From Generation to Generation55 Questions
Exam 4: Pedigree Analysis in Human Genetics60 Questions
Exam 5: Complex Patterns of Inheritance41 Questions
Exam 6: Cytogenetics: Karyotypes and Chromosome Aberrations59 Questions
Exam 7: Development and Sex Determination59 Questions
Exam 8: DNA Structure and Chromosomal Organization53 Questions
Exam 9: Gene Expression: From Genes to Proteins68 Questions
Exam 10: From Proteins to Phenotypes58 Questions
Exam 11: Mutation: the Source of Genetic Variation57 Questions
Exam 12: Genes and Cancer56 Questions
Exam 13: An Introduction to Genetic Technology45 Questions
Exam 14: Biotechnology and Society53 Questions
Exam 15: Genomes and Genomics50 Questions
Exam 16: Reproductive Technology, Genetic Testing, and Gene Therapy52 Questions
Exam 17: Genes and the Immune System62 Questions
Exam 18: Genetics of Behavior51 Questions
Exam 19: Population Genetics and Human Evolution71 Questions
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The main problem for sufferers of cystic fibrosis is
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(Multiple Choice)
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Correct Answer:
C
The gene responsible for Marfan syndrome encodes a protein associated with
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B
Which of the following is NOT a symptom of Marfan syndrome?
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Correct Answer:
D
The analysis of a pedigree is complete when the information in the pedigree supports the hypothesis formed by the geneticist.
(True/False)
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Which of the following is NOT a characteristic of an autosomal recessive trait?
(Multiple Choice)
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Mendel's laws apply to all sexually reproducing organisms. Therefore, the basic methods of genetic analysis in humans and other organisms is the same.
(True/False)
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Human traits are controlled only by the genetic material found in the 46 chromosomes.
(True/False)
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Two phenotypically normal parents have six children. Two daughters and two sons have the same genetic disease. This would be the expected situation for
(Multiple Choice)
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How would you distinguish between a trait that is X-linked dominant trait and one that is autosomal dominant?
(Short Answer)
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Approximately how many Y-linked genes have been discovered?
(Multiple Choice)
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Mitochondrial gene defects mainly cause myopathies (conditions affecting ____________________), and encephalomyopathies (conditions also affecting ____________________).
(Short Answer)
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The gene that codes for the connective tissue protein fibrillin is the gene that causes ____________________.
(Short Answer)
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Valeria has a serious disorder called fragile X syndrome and her brother does not have the disorder. Her mother does not have the disorder but her father does. What is the most likely inheritance pattern for fragile X syndrome?
(Multiple Choice)
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Adults who have children who have died from lethal recessive disorders are most likely ____________________.
(Short Answer)
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A defective form of the protein dystrophin is involved in the diseases __________ and ________.
(Short Answer)
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Is it easier to work out pedigrees for dominant traits than for recessive ones? What can complicate the analysis of dominant traits?
(Short Answer)
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Duchenne muscular dystrophy and Becker's muscular dystrophy represent allelic forms of the same X-linked gene.
(True/False)
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