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What is DNA, and How is it Used in Today’s Society?
What is DNA, and How is it Used in Today’s Society?

... • Developed by Gregor Mendel (1822-1884): studied heredity in pea plants (mainly texture and color of seeds); based solely on observations (no knowledge of DNA or meiosis) – see cartoon – Law of Segregation: there are two sets of genes for a particular trait (one from each parent), but only one gets ...
Document
Document

... • Begins with one diploid (2n) cell four haploid (n) cells. • Sex cells (gametes) haploid. • Sperm fertilizes an egg-results in zygote (diploid) • Zygote develops by MITOSIS into a multicellular organism. • Reproduction —Production and subsequent fusion of haploid sex cells. ...
An Aside: X Inactivation in Female Mammals
An Aside: X Inactivation in Female Mammals

... If a color blind man has children with a “wild-type” woman, what are the chances that a daughter of theirs will be colorblind? What are the chances that their son will be ...
RW - My CCSD
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Sex linked inheritance, sex linkage in Drosophila and man, XO, XY
Sex linked inheritance, sex linkage in Drosophila and man, XO, XY

... The X and Y chromosomes in humans differ in size and genetic ...
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How to be a clinical geneticist

... • All these 46 chromosomes contain all the information needed to create a whole baby • As the cells divide, the DNA is copied over and over into each new cell ...
The Origins of Variation
The Origins of Variation

... Still more chromosomal rearrangements Inversion - the flipping over (reverse orientation) of a DNA sequence one example known to have produced increased fertility in women Pericentric inversion – includes centromere Paracentric inversion – does not include centromere Unequal crossing over involving ...
Keystone Practice Questions #2 Cell Division, DNA
Keystone Practice Questions #2 Cell Division, DNA

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Chapter 12 - Cloudfront.net
Chapter 12 - Cloudfront.net

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Biology Chapter 10 Meiosis Notes 3-27

...  Shows chromosomal abnormalities o Number o Size/Structure Abnormal Chromosome Number Nondisjunction during Meiosis  Homologous chromosomes fail to separate during Anaphase I of Meiosis or Sister chromatids fail to separate during Anaphase II of Meiosis  Risks increase with mother’s age Most embr ...
Consortium for Educational Communication Summary
Consortium for Educational Communication Summary

... factors involved one each contributed by male and female parents during reproduction. The law of independent assortment states that the distribution of alleles to gametes during meiosis is random. If one particular allele goes to one gamete, it has no influence on the likelihood of any other allele ...
Lecture#18 - Sex chromosomes and sex linkage Concepts: In many
Lecture#18 - Sex chromosomes and sex linkage Concepts: In many

... Plants: Most have both male (stamens) and female (pistil) reproductive organs (called a hermaphrodite) and therefore we do not need to consider the determination of sex in plants Animals: Often, sex determination is due to, a pair of "sex" chromosomes. Note: 1- Not all species use chromosomes to det ...
Heredity in One Page - Lakewood City Schools
Heredity in One Page - Lakewood City Schools

... are then strung together into chains of protein by little structures called ribosomes. When a cell gets too big, it must divide. This process is called mitosis. In mitosis, each chromosome makes a copy of itself for the new cell. Therefore, each cell, which had all of its pairs of chromosomes (2n), ...
McCance: Pathophysiology, 6th Edition
McCance: Pathophysiology, 6th Edition

... 2. Humans have 23 pairs of chromosomes: 22 of these pairs are autosomes. The remaining pair consists of the sex chromosomes. Females have 2 homologous X chromosomes as their sex chromosomes; males have an X and a Y chromosome. 3. A karyotype is an ordered display of chromosomes arranged according to ...
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Chromosomes and Sex
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500 100 How Organisms Grow The Stages of Life Inherited

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MECHANISMS OF GENETIC CHANGE
MECHANISMS OF GENETIC CHANGE

... •Mutations can also take place in genes where the base sequence is changed due to substitution, addition or deletion of single bases. •Particular codons can also repeat themselves a number of times. •Base substitution affects only the triplet it takes place in. This may then affect one amino acid in ...
chromosome - TeacherWeb
chromosome - TeacherWeb

... Genetic disorder that consists of a broad spectrum of features that vary in individuals, but usually have the common findings of short stature (average adult height: 4 feet 8 inches) and loss of ovarian function. The loss of ovarian function usually leads to infertility and inhibited sexual developm ...
Reebops - Kennesaw State University | College of Science and
Reebops - Kennesaw State University | College of Science and

... of DNA. A gene is a segment of the long DNA molecule. Different genes may be different lengths. Each gene is a code for how a certain molecule can be made. The molecules produced by the genes can generally be sorted into two different types: ones that run the chemical reactions in your body, and one ...
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What are chromosomes?

... or short arms close to the centromere A relatively common Robertsonian translocation is between chromosome 14 and chromosome 21 In meiosis, a trivalent is formed. ...
Meiosis
Meiosis

... • Homologous chromosomes contain the same genes, ...
Genes are on chromosomes
Genes are on chromosomes

... -chromosomes said to segregate -genes on those chromosomes also said to segregate during meiosis Behavior of 2 different genes at different positions on the same chromosome -chromosomes go through meiosis ...
4-3 Challenge Practice Questions
4-3 Challenge Practice Questions

... When do chromosomes appear? • Chromosomes are only visible during cell division. ...
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Karyotype



A karyotype (from Greek κάρυον karyon, ""kernel"", ""seed"", or ""nucleus"", and τύπος typos, ""general form"") is the number and appearance of chromosomes in the nucleus of a eukaryotic cell. The term is also used for the complete set of chromosomes in a species, or an individual organism.Karyotypes describe the chromosome count of an organism, and what these chromosomes look like under a light microscope. Attention is paid to their length, the position of the centromeres, banding pattern, any differences between the sex chromosomes, and any other physical characteristics. The preparation and study of karyotypes is part of cytogenetics. The study of whole sets of chromosomes is sometimes known as karyology. The chromosomes are depicted (by rearranging a photomicrograph) in a standard format known as a karyogram or idiogram: in pairs, ordered by size and position of centromere for chromosomes of the same size.The basic number of chromosomes in the somatic cells of an individual or a species is called the somatic number and is designated 2n. Thus, in humans 2n = 46. In the germ-line (the sex cells) the chromosome number is n (humans: n = 23).p28So, in normal diploid organisms, autosomal chromosomes are present in two copies. There may, or may not, be sex chromosomes. Polyploid cells have multiple copies of chromosomes and haploid cells have single copies.The study of karyotypes is important for cell biology and genetics, and the results may be used in evolutionary biology (karyosystematics) and medicine. Karyotypes can be used for many purposes; such as to study chromosomal aberrations, cellular function, taxonomic relationships, and to gather information about past evolutionary events.
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