Table of contents
- 1. Introduction to Genetics51m
- 2. Mendel's Laws of Inheritance3h 37m
- 3. Extensions to Mendelian Inheritance2h 41m
- 4. Genetic Mapping and Linkage2h 28m
- 5. Genetics of Bacteria and Viruses1h 21m
- 6. Chromosomal Variation1h 48m
- 7. DNA and Chromosome Structure56m
- 8. DNA Replication1h 10m
- 9. Mitosis and Meiosis1h 34m
- 10. Transcription1h 0m
- 11. Translation58m
- 12. Gene Regulation in Prokaryotes1h 19m
- 13. Gene Regulation in Eukaryotes44m
- 14. Genetic Control of Development44m
- 15. Genomes and Genomics1h 50m
- 16. Transposable Elements47m
- 17. Mutation, Repair, and Recombination1h 6m
- 18. Molecular Genetic Tools19m
- 19. Cancer Genetics29m
- 20. Quantitative Genetics1h 26m
- 21. Population Genetics50m
- 22. Evolutionary Genetics29m
2. Mendel's Laws of Inheritance
Probability and Genetics
3:28 minutes
Problem 25a
Textbook Question
Textbook QuestionA 'wrongful birth' case was recently brought before a court in which a child with Smith–Lemli–Opitz syndrome was born to apparently healthy parents. This syndrome is characterized by a cluster of birth defects including cleft palate, and an array of problems with the reproductive and urinary organs. Originally considered by their physician as having a nongenetic basis, the parents decided to have another child, who was also born with Smith–Lemli–Opitz syndrome. In the role of a genetic counselor, instruct the court about what occurred, including the probability of the parents having two affected offspring, knowing that the disorder is inherited as a recessive trait. What is the probability that one of them is a carrier and the other is not? [Hint: The p values in (b), (c), and (d) should equal 1.]
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Key Concepts
Here are the essential concepts you must grasp in order to answer the question correctly.
Recessive Inheritance
Recessive inheritance occurs when a trait is expressed only when an individual has two copies of the recessive allele. In the case of Smith–Lemli–Opitz syndrome, both parents must carry one copy of the mutated gene for their child to be affected. If both parents are carriers, there is a 25% chance with each pregnancy that their child will inherit the disorder.
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Carrier Probability
A carrier is an individual who has one copy of a recessive allele but does not express the trait. In this scenario, if both parents are carriers of the Smith–Lemli–Opitz syndrome gene, the probability that one parent is a carrier while the other is not can be calculated using Mendelian genetics. If one parent is a carrier (1/2 chance) and the other is not (1/2 chance), the overall probability is 1/2.
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Punnett Square
A Punnett square is a diagram used to predict the genetic makeup of offspring from two parents. It helps visualize the combinations of alleles that can result from a cross. In this case, constructing a Punnett square for the two carrier parents would show the probabilities of having affected, carrier, or unaffected children, aiding in understanding the likelihood of having two children with the syndrome.
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