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Introduction to Genetics using Punnett Squares
Introduction to Genetics using Punnett Squares

... Gregor Mendel was an Austrian monk and is known as the Father of Genetics.  Mendel was the gardener and observed that many of the plants looked different even though they were the same species.  He studied pea plants and their traits to see how they were passed on. This lead to our basic understan ...
Sordaria
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... chromatid of a synapsed tetrad to be followed through the entire meiotic process, including the events of recombination and crossing over if they occur. Two major types of important information can be obtained in this way. The first (using ordered tetrad analysis) allows identification of which two ...
Chapter 9 Genetics
Chapter 9 Genetics

... iii. The same phenotype may be determined by more than one genotype. d. A sperm or egg carries only one allele for each inherited character because allele pairs separate (segregate) from each other during the production of gametes. This statement is called the law of segregation. i. The fusion of ga ...
Blueprint of Life
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...  This occurs within a species and between species. If a new species is introduced into an area then the competition may lead to different species using different resources.  Resources can include food, space or mates. If populations that live in the same area could specialise on slightly different ...
ANSWERS TO REVIEW QUESTIONS
ANSWERS TO REVIEW QUESTIONS

... habilis, Homo erectus, Homo sapiens idaltu, Denisova hominin, Neanderthals. Overlaps are uncertain due to incomplete evidence. 2. Hominoids are ancestral to apes and humans, whereas hominins are ancestral to humans only. Therefore, hominoids are more ancient. 3. Physically, chimpanzees are not as si ...
Meiosis - greenebio
Meiosis - greenebio

... Chromatid homologous pairs align along the equator of the cell. This is random and results in Genetic variation Homologous – a chromosome with the same gene sequence as another, one is paternal and the other is maternal ...
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... A) Centromeres C) Chiasma ...
Chromothripsis: how does such a catastrophic event impact human
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Sex for the purposes of this class refers to 4 components
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Zoo/Bot 3333
Zoo/Bot 3333

... 3. A single crossover involving the inverted region on one chromosome and the homologous region on the other chromosome would yield an acentric fragment. a) 1 and 2; b) 1 and 3; c) 2 and 4; d) 1 and 4; e) none of the above. 4. A child was born with trisomy 18. When a gene on chromosome 18 was examin ...
Key for Exam 2 Part 1 - Evolutionary Biology
Key for Exam 2 Part 1 - Evolutionary Biology

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Chapter 7: Extending Mendelian Genetics
Chapter 7: Extending Mendelian Genetics

... The brown allele is always dominant over the blue allele so even if a person is heterozygous (one brown and one blue allele) for the bey 2 gene on chromosome 15 the brown allele will be expressed. The gey gene also has two alleles, one green and one blue. The green allele is dominant to the blue al ...
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Designer Genes - Heredity
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... Linkage – genes on the same chromosome inherited as a group Sex-linkage – genes on sex chromosomes (esp. X) Y-chromosome shorter – some genes from X missing X-linked traits more common in men Men get X-chromosome from mom Red-green colorblindness, hemophilia ...
Chapter 11: Intro. to Genetics
Chapter 11: Intro. to Genetics

... Summary of Mendel’s Principles • 1. traits are determined by genes from parents to offspring. • 2. when present a dominant trait will always show up. 2 recessive traits must exist together for recessive to show up. • 3. each adult has two copies of a gene (one from each parent). These genes segrega ...
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The Cell Cycle

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... 3. How are structure and function related in biology? Structure and function are related at the level of chemicals in cells. Different types of cells have different functions that depend on their specialized structures (i.e. brain cells have branches that receive info from other cells). Structure an ...
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Chapter 1 Biology Exam Study Guide

... 3. How are structure and function related in biology? Structure and function are related at the level of chemicals in cells. Different types of cells have different functions that depend on their specialized structures (i.e. brain cells have branches that receive info from other cells). Structure an ...
7.27 Spring 2006 PROBLEM SET DUE MAY 12, 2006 1. A couple
7.27 Spring 2006 PROBLEM SET DUE MAY 12, 2006 1. A couple

... an unbalanced translocation involving chromosomes 8 and 21. The fetus has a severe heart defect and does not survive to term. A karyotype is performed on both the mother and the father. The father is discovered to carry a balanced translocation between chromosomes 8 and 21 while the mother’s karyoty ...
[ the current understanding of DNA has changed dramatically from
[ the current understanding of DNA has changed dramatically from

... levels within the same species. Fireweed (Chamerion angustifolium) is an example of a plant species within which both diploid and tetraploid individuals can be ...
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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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