Table of contents
- 1. Introduction to Biology2h 40m
- 2. Chemistry3h 40m
- 3. Water1h 26m
- 4. Biomolecules2h 23m
- 5. Cell Components2h 26m
- 6. The Membrane2h 31m
- 7. Energy and Metabolism2h 0m
- 8. Respiration2h 40m
- 9. Photosynthesis2h 49m
- 10. Cell Signaling59m
- 11. Cell Division2h 47m
- 12. Meiosis2h 0m
- 13. Mendelian Genetics4h 41m
- Introduction to Mendel's Experiments7m
- Genotype vs. Phenotype17m
- Punnett Squares13m
- Mendel's Experiments26m
- Mendel's Laws18m
- Monohybrid Crosses16m
- Test Crosses14m
- Dihybrid Crosses20m
- Punnett Square Probability26m
- Incomplete Dominance vs. Codominance20m
- Epistasis7m
- Non-Mendelian Genetics12m
- Pedigrees6m
- Autosomal Inheritance21m
- Sex-Linked Inheritance43m
- X-Inactivation9m
- 14. DNA Synthesis2h 27m
- 15. Gene Expression3h 20m
- 16. Regulation of Expression3h 31m
- Introduction to Regulation of Gene Expression13m
- Prokaryotic Gene Regulation via Operons27m
- The Lac Operon21m
- Glucose's Impact on Lac Operon25m
- The Trp Operon20m
- Review of the Lac Operon & Trp Operon11m
- Introduction to Eukaryotic Gene Regulation9m
- Eukaryotic Chromatin Modifications16m
- Eukaryotic Transcriptional Control22m
- Eukaryotic Post-Transcriptional Regulation28m
- Eukaryotic Post-Translational Regulation13m
- 17. Viruses37m
- 18. Biotechnology2h 58m
- 19. Genomics17m
- 20. Development1h 5m
- 21. Evolution3h 1m
- 22. Evolution of Populations3h 52m
- 23. Speciation1h 37m
- 24. History of Life on Earth2h 6m
- 25. Phylogeny2h 31m
- 26. Prokaryotes4h 59m
- 27. Protists1h 12m
- 28. Plants1h 22m
- 29. Fungi36m
- 30. Overview of Animals34m
- 31. Invertebrates1h 2m
- 32. Vertebrates50m
- 33. Plant Anatomy1h 3m
- 34. Vascular Plant Transport2m
- 35. Soil37m
- 36. Plant Reproduction47m
- 37. Plant Sensation and Response1h 9m
- 38. Animal Form and Function1h 19m
- 39. Digestive System10m
- 40. Circulatory System1h 57m
- 41. Immune System1h 12m
- 42. Osmoregulation and Excretion50m
- 43. Endocrine System4m
- 44. Animal Reproduction2m
- 45. Nervous System55m
- 46. Sensory Systems46m
- 47. Muscle Systems23m
- 48. Ecology3h 11m
- Introduction to Ecology20m
- Biogeography14m
- Earth's Climate Patterns50m
- Introduction to Terrestrial Biomes10m
- Terrestrial Biomes: Near Equator13m
- Terrestrial Biomes: Temperate Regions10m
- Terrestrial Biomes: Northern Regions15m
- Introduction to Aquatic Biomes27m
- Freshwater Aquatic Biomes14m
- Marine Aquatic Biomes13m
- 49. Animal Behavior28m
- 50. Population Ecology3h 41m
- Introduction to Population Ecology28m
- Population Sampling Methods23m
- Life History12m
- Population Demography17m
- Factors Limiting Population Growth14m
- Introduction to Population Growth Models22m
- Linear Population Growth6m
- Exponential Population Growth29m
- Logistic Population Growth32m
- r/K Selection10m
- The Human Population22m
- 51. Community Ecology2h 46m
- Introduction to Community Ecology2m
- Introduction to Community Interactions9m
- Community Interactions: Competition (-/-)38m
- Community Interactions: Exploitation (+/-)23m
- Community Interactions: Mutualism (+/+) & Commensalism (+/0)9m
- Community Structure35m
- Community Dynamics26m
- Geographic Impact on Communities21m
- 52. Ecosystems2h 36m
- 53. Conservation Biology24m
13. Mendelian Genetics
Sex-Linked Inheritance
0:29 minutes
Problem 15a
Textbook Question
Textbook QuestionTwo mothers give birth to sons at the same time in a busy hospital. The son of couple 1 is afflicted with hemophilia A, which is a recessive X-linked disease. Neither parent has the disease. Couple 2 has a normal son even though the father has hemophilia A. The two couples sue the hospital in court, claiming that a careless staff member swapped their babies at birth. You appear in court as an expert witness. What do you tell the jury? Make a diagram that you can submit to the jury.
Verified step by step guidance
1
Step 1: First, let's understand the basics of hemophilia A. Hemophilia A is a genetic disorder that is X-linked recessive. This means that the disease is carried on the X chromosome and is recessive, meaning that two copies of the defective gene are needed for the disease to manifest. In males, who have only one X chromosome, one copy of the defective gene is enough to cause the disease.
Step 2: Now, let's consider the first couple. The son has hemophilia A, but neither parent has the disease. This is possible if the mother is a carrier of the disease, meaning she has one copy of the defective gene and one normal gene. She can pass the defective gene to her son, who will then have the disease. The father, having a normal X chromosome, cannot be the source of the defective gene.
Step 3: For the second couple, the father has hemophilia A, but the son is normal. This is also possible. The father can only pass his Y chromosome to his son, so the son cannot inherit the disease from him. The mother, who is assumed to be normal, provides a normal X chromosome to the son.
Step 4: Based on this information, there is no evidence to suggest that the babies were swapped at birth. The genetic outcomes are consistent with the parents' genotypes and the nature of X-linked recessive inheritance.
Step 5: To illustrate this, we can draw a Punnett square for each couple. For couple 1, the square would show that half of the sons would have hemophilia A if the mother is a carrier. For couple 2, the square would show that none of the sons would have hemophilia A, as the father can only pass on his Y chromosome.
Recommended similar problem, with video answer:
Verified Solution
Video duration:
29sPlay a video:
Related Videos
Related Practice