Biology
Biology
12th Edition
ISBN: 9780134813448
Author: Audesirk, Teresa, Gerald, Byers, Bruce E.
Publisher: Pearson,
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Chapter 10, Problem 3MC
Summary Introduction

Introduction: Chromosomes are long thread-like structures that carry coded genetic information in the form of nucleotide sequences in DNA. They are transferred from one generation to succeeding generation by the process of sexual reproduction.

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Crossing over usually contributes to genetic variation by exchanging chromosomal segments between:   A. nonhomologous loci of the genome (E) autosomes and sex chromosomes.   B. chromatids of nonhomologous chromosomes   C. non-sister chromatids of homologous chromosomes   D. sister chromatids of a chromosome   E. polyploid chromosomes
What is the fundamental difference between mitosis and meiosis?   A. DNA is replicated twice in meiosis, but only once in mitosis.   B. The number of DNA molecules per cell nucleus is cut in half in meiosis but remains constant in mitosis.   C. The number of chromosomes doubles in meiosis, whereas it stays the same in mitosis.     D. Mitosis involves two cell divisions, whereas meiosis only involves one.
An error occurred during meiotic cell division, and a human egg has an extra copy of chromosome 21. That egg was fertilized by a normal sperm to create an embryo. This would lead to an individual A) who was tetraploid B) who would be normal in chromosomal number C) who had trisomy D) who was triploid
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Mitochondrial mutations; Author: Useful Genetics;https://www.youtube.com/watch?v=GvgXe-3RJeU;License: CC-BY