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Genetic Technology PPT
Genetic Technology PPT

... In order to study these disorders, cells from a person are grown with a chemical that stops cell division at the metaphase stage a. During metaphase, a chromosome exists as two chromatids attached at the centromere. 2. The cells are stained to reveal banding patterns and placed on glass slides. 3. T ...
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relates Mendel`s discoveries to actual behavior of chromosomes

... Thomas Hunt Morgan- first person to associate a specific gene with a specific chromosome by using a species of fruit flies (to take advantage of its ability to produce hundreds of offspring from one mating, and its having only four pairs of chromosomes) A. Wild Type- the normal phenotype for a chara ...
study guide2 Sp12
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Genetics Power point
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... This involves catching the chromosomes when they are compacted ready for cell division. Then they must be paired up with their “match” When all the chromosomes in the human genetic makeup are paired, it looks like this: For simplicity, geneticist only use one half of each of the Chromosome to do the ...
Name: Date: Class Period: Meiosis and Mendelian Genetics
Name: Date: Class Period: Meiosis and Mendelian Genetics

... dimpled chin is a trait that is only controlled by one gene, meaning that there is one location (loci) on this homologous pair of chromosomes that is for the dimpled chin gene. There are no other genes anywhere, on any chromosome, that control the dimpled chin trait. Some traits, like height and ski ...
Unit I: Genes, Nucleic A...d Chromosomes - BioWiki
Unit I: Genes, Nucleic A...d Chromosomes - BioWiki

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interphase prophase metaphase anaphase telophase cytokinesis
interphase prophase metaphase anaphase telophase cytokinesis

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Chapter 1 Art Slides
Chapter 1 Art Slides

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Genes
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Introducing Variation
Introducing Variation

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Paterns of Inheritance I
Paterns of Inheritance I

... Mendelian genes have specific loci on chromosomes, and it is the chromosomes that undergo segregation and independent assortment Theory of segregation – diploid cells have pairs of genes, on pairs of homologous chromosomes. During meiosis, the two genes of each pair segregates from each other, and e ...
Monohybrid Crosses & Phenotypes and Genotypes
Monohybrid Crosses & Phenotypes and Genotypes

... Example-blood type in humans a. blood type is determined by presence or absence of proteins on the surface of red blood cells ...
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why care

... Independent Assortment. Independent assortment produces 2n different possible gametes, where n = the number of unique chromosomes. In humans, n = 23 and 223 = ...
BIOLOGY EOC PRACTICE TEST _1[1]
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Biological Terminology (Bio Terms)
Biological Terminology (Bio Terms)

... Biology students are faced with the challenge of learning a large number of new terms predominately based on the Latin and Greek languages. Therefore, students should learn to recognize word parts since they often give clues as to the meaning of a word. Research suggests that students knowledgeable ...
Human Genetics
Human Genetics

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Genetic_Meiosis Review_15
Genetic_Meiosis Review_15

... 8. _______________ The form of the trait that will only be expressed if there are two homozygous alleles; represented by a lower case letter. 9. _______________ The two pure-breeding plants that Mendel first crossed to form a hybrid F1 generation. 10. _______________ Different forms of the same gene ...
GENETICS 310
GENETICS 310

... B  A  purebred  female  from  colony  1  is  crossed  to  a  homozygous  male  from  colony  2  and  the   F1  progeny  are  viable.    Show  how  F1  chromosomes  will  appear  at  synapsis  in  meiosis1.       ...
COMPLEX PATTERNS OF INHERITANCE
COMPLEX PATTERNS OF INHERITANCE

... during egg formation, sperm formation, or early stages of embryo growth alters gene expression in a way that is fixed during an individual’s lifetime  Permanently affect the phenotype of the individual, but they are not permanent over the course of many generations and they do not change the actual ...
Genetics - Tour of the Basics
Genetics - Tour of the Basics

... you’re a fish or a fly, or a human. Each human cell has __________ chromosomes. All the DNA is organized into two sets of __________ chromosomes. We get genetic material from both of our _______________ - that’s why children look like both their mom and dad. ...
Chromosome Variations
Chromosome Variations

... If mispairing in meiosis occurs, followed by a crossover between delta and beta, the hemoglobin variant Hb-Lepore is formed. This is a gene that starts out delta and ends as beta. Since the gene is controlled by DNA sequences upstream from the gene, Hb-Lepore is expressed as if it were a delta. That ...
Let` review answers as a class.
Let` review answers as a class.

... Complete the notes on your “Chromosomes and Sex-Linked Traits” worksheet. If we take all the chromosomes out of one cell and match them up, we find that we have 23 pairs. The first 22 pairs contain the genes that make up our bodies (called autosomes). The 23rd pair are called sex chromosomes becaus ...
Plant DNA mini
Plant DNA mini

... these organisms are likely to be novel and of significant biological interest. Additionally, their identification may have practical benefits, contributing to our understanding of human disease genes and providing useful tools for agricultural bioengineering. ...
File - Mrs. Harlin`s Website
File - Mrs. Harlin`s Website

... incorrectly, resulting in faulty proteins. These mutations can cause disorders that may or may not be lethal. ...
Chapter 13
Chapter 13

... called a locus on a certain chromosome ...
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Ploidy



Ploidy is the number of sets of chromosomes in a cell. Usually a gamete (sperm or egg, which fuse into a single cell during the fertilization phase of sexual reproduction) carries a full set of chromosomes that includes a single copy of each chromosome, as aneuploidy generally leads to severe genetic disease in the offspring. The gametic or haploid number (n) is the number of chromosomes in a gamete. Two gametes form a diploid zygote with twice this number (2n, the zygotic or diploid number) i.e. two copies of autosomal chromosomes. For humans, a diploid species, n = 23. A typical human somatic cell contains 46 chromosomes: 2 complete haploid sets, which make up 23 homologous chromosome pairs.Because chromosome number is generally reduced only by the specialized process of meiosis, the somatic cells of the body inherit and maintain the chromosome number of the zygote. However, in many situations somatic cells double their copy number by means of endoreduplication as an aspect of cellular differentiation. For example, the hearts of two-year-old children contain 85% diploid and 15% tetraploid nuclei, but by 12 years of age the proportions become approximately equal, and adults examined contained 27% diploid, 71% tetraploid and 2% octaploid nuclei.Cells are described according to the number of sets present (the ploidy level): monoploid (1 set), diploid (2 sets), triploid (3 sets), tetraploid (4 sets), pentaploid (5 sets), hexaploid (6 sets), heptaploid or septaploid (7 sets), etc. The generic term polyploid is frequently used to describe cells with three or more sets of chromosomes (triploid or higher ploidy).
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