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... XXY = Klinefelter’s syndrome male XXX = Trisomy X female XYY = Jacob’s syndrome male XO = Turner syndrome female ...
Biology 1406 Exam 4 Notes Cell Division and
Biology 1406 Exam 4 Notes Cell Division and

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EOC Study Guide final doc printer friendly FINAL

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Big Idea 16 : Heredity and Reproduction
Big Idea 16 : Heredity and Reproduction

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ANSWERS - midterm study guide
ANSWERS - midterm study guide

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6 Meiosis and Mendel - Speedway High School

... Although each chromosome in a homologous pair has copies of the same genes, the two copies may differ. For example, each chromosome in a pair might have a gene that influences eye color. But the gene on one chromosome of the pair may lead to brown eyes and the gene on the other chromosome may lead ...
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GENERAL PATHOLOGY Genetic disorders: Introduction: DNA

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Heredity

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... Chapter 8 Check List • 1) _____________ -is the process of passing traits from parents to offspring. • 2) The genetic makeup or genes of an organism is called its _________________. • 3) _________ determines the inherited traits of an organism. • 4) ______________ - is the way an organism looks and ...
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Human Inheritance

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File

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Control of Chromosome Pairing and Genome Evolution in Disomic

... In the AC and CA polyploids, no directional change was observed. They suggested that the difference between the AB/BA and AC/CA polyploids was due to the fact that the A and C genomes are more closely related than are the A and B genomes. Implications of results: ...
Lecture #11 - Suraj @ LUMS
Lecture #11 - Suraj @ LUMS

... homologous sets of chromosomes (2n). Almost all cells in our body are diploid . In humans the diploid number (2n) is 46. • Haploid Cells: Cells whose nuclei contain a single set of chromosomes (n). Egg and sperm cells are haploid. In humans the haploid number (n) is 23. • Fertilization: Haploid egg ...
pedigree - Mrs. Salmon Science
pedigree - Mrs. Salmon Science

... more than normal. Note the recessive x on the mother. Because males get one x they are Much more likely to have this trait. ...
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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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