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Chapter 5 - SchoolRack
Chapter 5 - SchoolRack

... What does that mean? Mendel decided that meant that one alleles was dominant and the other allele ...
A BIT ON DROSOPHILA GENETICS AND NOMENCLATURE
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... chromosomes. In Drosophila, sex is determined by the ratio of X chromosomes to autosomal sets. A ratio of 0.5 (one X to two autosomes) produces males while a ratio of 1.0 (two X to two autosomes) produces females. The Y chromosome contains few genes and is not required for most aspects of male devel ...
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... can alter phenotype because a gene’s expression is influenced by its location. Copyright © 2002 Pearson Education, Inc., publishing as Benjamin Cummings ...
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... • Sex-linked genes may be on the X chromosome (Xlinkage) or the Y chromosome (Y- linkage). The X chromosome carries many such genes, the Y chromosome has very few. • In humans, features linked on the Y chromosome will only arise in males, whereas features linked on the X chromosome may arise in eith ...
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... chromosome is passed along as a unit. • Results of crosses with linked genes deviate from those expected according to independent assortment. Copyright © 2002 Pearson Education, Inc., publishing as Benjamin Cummings ...
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... • A test of the chromosome theory • If genes are on specific chromosomes, then traits determined by the gene should be transmitted with the chromosome. • T.H. Morgan’s experiments demonstrating sex-linked inheritance of a gene determining eye-color demonstrate the transmission of traits with chromos ...
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... chromosome XVI, nucleotide coordinates 731,001–860,000, where regions are duplicated onto a 129.5-kb section on the right arm of chromosome VII (nucleotide coordinates 648,001–777,500). Although removed from the comparison that identified this duplication, the region on chromosome XVI is rich in rep ...
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... 12. How does the DNA code for hemoglobin in a sickle cell individual differ from the hemoglobin gene in a normal individual? Explain what symptoms occur because of this mutation. 13. What are the 4 possible blood types a person can have? Give an example of a cross between 2 different blood typed ind ...
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... The first generation • Mendel selected a six-foot-tall pea plant that came from a population of pea plants, all of which were over six feet tall. • He cross-pollinated this tall pea plant with pollen from a short pea plant. • All of the offspring grew to be as tall as the taller parent. ...
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... -The first phase, chromosome mapping, which seeks to identify the relevant chromosome and rough position of the gene of interest. -The second phase, interval mapping, seeks to place the gene of interest in an interval between two SNPs, and can be used iteratively to fine map the gene. (PMID: 161569 ...
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... Aneuploids give rise to aneuploid clones ...
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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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