Which of the following ways reciprocal translocated chromosomes are sorted produces viable gametes?
Table of contents
- 1. Introduction to Genetics42m
- 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: Translocations
Multiple Choice
How many chromosomes does a person who is a carrier for familial down syndrome caused by a robertsonian translocation have?
A
45
B
46
C
47
D
48
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Verified step by step guidance1
Understand that familial Down syndrome can be caused by a Robertsonian translocation, which involves the fusion of two acrocentric chromosomes.
Recognize that in a typical human karyotype, there are 46 chromosomes, including 22 pairs of autosomes and 1 pair of sex chromosomes.
In a Robertsonian translocation, two acrocentric chromosomes fuse at the centromere, reducing the total chromosome count by one.
A carrier of familial Down syndrome has one chromosome pair replaced by a single translocated chromosome, resulting in a total of 45 chromosomes.
Consider that the carrier is phenotypically normal because they have the correct amount of genetic material, despite having fewer chromosomes.
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