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Human Anatomy & Physiology (11th Edition)
11th Edition
ISBN: 9780134580999
Author: Elaine N. Marieb, Katja N. Hoehn
Publisher: PEARSON
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How do genes and chromosomes share similarity from the point of view of genitical studies?
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- A scientist investigating the genome of two related individuals observes a difference of a few nucleotides in one individual compared to the other. The nucleotide differences are in a region of noncoding DNA on chromosome 1. Would these differences be considered a mutation? Why or why not? Yes, the difference in nucleotide sequences between the individuals is a mutation because it will affect the phenotype of the two individuals. Yes, any heritable variation in the nucleotide sequence is considered a mutation, even if that variation is in a noncoding region of DNA. Not enough information was provided to determine if this nucleotide difference is a mutation because the effect on phenotype is unknown. No, the change in nucleotide sequence doesn't appear in a coding region of the DNA and so can't be a mutation.arrow_forwardHow is it possible for humans to differ genetically from each other if we all have the same genes arranged in the same order on our chromosomes?arrow_forwardWhat is it that forms the basis of DNA fingerprinting?arrow_forward
- How to Identify structural sequences, such as telomericsequences, in chromosomes ?arrow_forwardGenes A and B are 7.5 map units apart on one chromosome. Genes C and D are 8.0 map units apart on a second non-homologous chromosome. • The recombination frequency between A and B is? • The recombination frequency between A and C is? • The recombination frequency between C and D is? • The recombination frequency between B and D is?arrow_forward
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