Recording-2025-02-27T17:36:44

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16 Terms

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Diploid

A cell or organism that has two sets of chromosomes, one from each parent, represented as 2n (e.g., humans have 46 chromosomes).

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Haploid

A cell or organism that has one set of chromosomes, represented as n (e.g., gametes such as sperm and egg cells, which have 23 chromosomes in humans).

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Zygote

The fertilized egg that results from the union of a sperm cell and an egg cell, which is diploid (2n).

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Homologous Chromosomes

A pair of chromosomes, one from each parent, that are similar in shape, size, and genetic content.

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Autosomes

The 22 pairs of chromosomes in humans that do not determine sex, as opposed to sex chromosomes (X and Y).

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Sex Chromosomes

The chromosomes that determine the biological sex of an individual (X and Y in humans).

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Mitosis

A type of cell division that results in two daughter cells with the same number of chromosomes as the parent cell (diploid).

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Meiosis

A specialized type of cell division that produces haploid gametes (sperm and egg), involving two rounds of cell division and genetic recombination.

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Crossing Over

The exchange of genetic material between homologous chromosomes during prophase I of meiosis, leading to genetic variation.

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Independent Assortment

The random arrangement of homologous chromosome pairs during metaphase I of meiosis, resulting in genetic variation.

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Alleles

Different forms of a gene that can exist at a specific locus on a chromosome, contributing to genetic diversity.

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Gametes

Reproductive cells (sperm and eggs) that are haploid and unite during fertilization to form a zygote.

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Menopause

The time in a woman's life when she ceases to produce eggs, marking the end of her reproductive years.

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Sister Chromatids

Identical copies of a chromosome that are connected by a centromere; they are formed during DNA replication.

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Genetic Variation

The diversity in gene frequencies among individuals within a population, generated through meiosis and sexual reproduction.

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Locus

The specific physical location of a gene or a significant sequence on a chromosome.