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Educational flashcards covering the fundamental concepts of chromosomes, including prokaryotic vs. eukaryotic structures, ploidy, and karyotype analysis based on IB Biology standards.
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Chromosomes
Structures that contain genes shared by the members of the same species.
Prokaryotic Chromosome
A chromosome consisting of a circular molecule of ADN (DNA).
Plasmids
Small, additional molecules of ADN (DNA) that contain genes useful for the cell (such as antibiotic resistance) but are not necessary for basic processes.
Eukaryotic Chromosomes
Linear molecules of ADN (DNA) associated with histone proteins.
Genes
Small sections of chromosomes that code for the production of different proteins, which are later translated into different phenotypes or traits.
Sister Chromatids
Two identical molecules of ADN (DNA) produced by replication.
Centromere
The location where two sister chromatids join together; its position can range from one end to the center of the chromosome.
Homologous Chromosomes
Chromosomes that have the same sequence of genes but not necessarily the same alleles of those genes.
Haploid Nucleus
A nucleus that has one chromosome of each pair; in humans, these contain 23 chromosomes.
Gametes
Sexual cells, such as the ovum and sperm, that possess haploid nuclei and fuse during sexual reproduction.
Diploid Nucleus
A nucleus that has two chromosomes of each type, representing two complete sets of the chromosomes found in the species; in humans, these contain 46 chromosomes.
Chromosome Number
A characteristic trait of the members of a species; organisms with different numbers of chromosomes are unlikely to be able to interbreed.
Sex Chromosomes
The pair of chromosomes (23 in humans) that determine the sex of an individual, such as X and Y.
Autosomes (Somatic Chromosomes)
Chromosomes that do not determine sex; in humans, these are chromosome pairs 1 through 22.
Karyogram
An image of the chromosomes of an organism arranged in homologous pairs of decreasing length.
Karyotype
The description of the specific number and type of chromosomes present in an organism; a normal human karyotype shows 46 chromosomes in 23 pairs.
Down Syndrome (Trisomy 21)
A chromosomal anomaly where there are three copies of chromosome 21 instead of two.
Turner Syndrome (Monosomy X)
A chromosomal anomaly characterized by the total or partial absence of the X chromosome.
Klinefelter Syndrome
A chromosomal anomaly designated as XXY.