A healthy couple with a history of three previous spontaneous abortions has just had a child with cri-du-chat syndrome, a disorder caused by a terminal deletion of chromosome 5. Their physician orders karyotype analysis of both parents and of the child. The karyotype results for chromosomes 5 and 12 are shown here. Why does this parent have a normal phenotype?
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
6. Chromosomal Variation
Chromosomal Rearrangements: Deletions
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Join thousands of students who trust us to help them ace their exams!Watch the first videoMultiple Choice
In the context of chromosomal rearrangements, what is the most accurate description of what happens when a piece of DNA is missing from a chromosome?
A
A deletion occurs, removing one or more genes from the chromosome, which can change gene dosage and phenotype.
B
An inversion occurs, reversing the orientation of a chromosomal segment without changing the total amount of DNA.
C
A duplication occurs, producing an extra copy of a chromosomal segment and increasing gene dosage.
D
A balanced reciprocal translocation occurs, exchanging segments between nonhomologous chromosomes without net loss of DNA.
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Chromosomal Rearrangements: Deletions practice set

