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BioH_Cell Division
BioH_Cell Division

... Meiosis requires two stages (meiosis I & II) in order to reduce the chromosome count of a diploid stem cell within the ovaries or testis to the haploid number. Meiosis I is preceded by an interphase similar to that which precedes mitosis. ...
Chapter 12 Section 3-Codominance in Humans
Chapter 12 Section 3-Codominance in Humans

... Weak muscles through out body Short, wide neck with excess skin Short/stocky arms & legs Facial features: sm. Low set ears/nasal bridge pushed in/ irregular mouth & tongue ...
RF (mu) = NPD + ½(T)/total x 100
RF (mu) = NPD + ½(T)/total x 100

... Behavioral isolation: Species engage in distinct courtship and mating rituals (see Figure 1). Mechanical isolation: Interbreeding is prevented by structural or molecular blockage of the formation of the zygote. Mechanisms include the inability of the sperm to bind to the egg in animals, or the femal ...
Patterns of inheritance
Patterns of inheritance

... exceptions to this rule are the sex chromosomes that determine sex in a given species. For example, in the XY system that is found in most mammals - including human beings - males have one X chromosome and one Y chromosome (XY) and females have two X chromosomes (XX). The paired chromosomes that are ...
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03HeredityEnvironment2

... Allele = Slight normal variation in a gene ...
12 Units of Heredity
12 Units of Heredity

... Aneuploidy  and  Cancer   •  Aneuploidy  can  occur   during  mitosis   –  Has  less  of  an  effect  because   cells  can  be  eliminated  (final   check  point  of  mitosis)   ...
Slide 1
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Genetics
Genetics

... Meiosis I: Normal ...
File
File

... 1. What is a karyotype used for?  To look at the chromosomes to see if they are normal in number – there should be 46 (23 pairs). If there are too many or too few it reveals that there is a genetic disorder. 2. What is a pedigree chart, and what is it used for?  A chart that shows how a genetic di ...
Cytogenetics
Cytogenetics

... Loss or gain of a single chromosome(s) Results from errors in division during meiosis, where a daughter cell receives both pairs of a particular chromosome (nondisjunction errors). Addition of an extra chromosome, trisomy, has been described for all the chromosomes but only three autosomal trisomies ...
Notes - J Co Review
Notes - J Co Review

... • Human chromosomes can be mapped out in a chart called a karyotype • Everybody’s first 22 chromosomes are structurally identical o They appear as two homologous X’s • However, the structure of the 23rd chromosome differs between males and females o It appears as two X’s in females, and an X and a Y ...
Basic Concepts of Human Genetics
Basic Concepts of Human Genetics

... sperm), which are produced by sex organ. 3. Gametes are produced by a special cell division called Meiosis. 4. Meiosis gives rise to daughter cells (ovum or sperm) which contain only a haploid (single chromosome, not pair) set of 22 autosomes and a sex chromosome. ...
Chapter 8: Cell Division
Chapter 8: Cell Division

... Chapter 11: Gene Expression 1. Understand the two-step process of protein synthesis (transcription and translation); also define what a protein is. 2. Know the difference between DNA and RNA. 3. Know the three different types of RNA. 4. Know what codons are and their role in determining the amino ac ...
Unexpected Resilience of TSD species at the
Unexpected Resilience of TSD species at the

... The Y chromosome has already disappeared in some mammals o Just because the chromosome has gone so long without losing genes doesn’t mean it couldn’t lose them tomorrow Other interesting facts: o The Y chromosome regulates genes differently than the X chromosome which can lead to important consequen ...
Ch 15: Chromosomal Basis of Inheritance
Ch 15: Chromosomal Basis of Inheritance

... Mendel & Chromosomes • Mendel was ahead of his time. 19th C cytology suggested a mechanism for his earlier findings. What did they find?  Chromosomes and genes are both present in pairs in diploid cells.  Homologous chromosomes separate and alleles segregate during meiosis.  Fertilization restor ...
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... It depends on the nature of the gene’s protein product and its role in the cell. ...
DNA Discovery
DNA Discovery

... • The individual grains are purple with white streaks or mottling. This mottling effect defies Mendel's basic principles of genetics because individual grains may be multicolored rather than a single color. • In the pigmented layer of corn grains, the position of transposons may inhibit or block pig ...
6.2 Human Genetic Disorders
6.2 Human Genetic Disorders

... 7.2.d Students know plant and animal cells contain many thousands of different genes and typically have two copies of every gene. The two copies (or alleles) of the gene may or may not be identical, and one may be dominant in determining the phenotype while the other is recessive. ...
CHAPTER 14 THE HUMAN GENOME
CHAPTER 14 THE HUMAN GENOME

... - an absent or faulty gene is replaced by a normal, working gene - can be used to correct genetic disorders - the normal gene can make the correct protein or enzyme and eliminate the cause of the disorder - viruses are modified so they do not cause disease and genetically engineered to carry the nor ...
Part 1 – Genetics 101
Part 1 – Genetics 101

... depend on whether the pathological gene comes from the mother or the father. Ex. : Prader-Willi Syndrome or Angelman Syndrome Prader Willi Syndrome is caused by a microdeletion on the chromosome 15, that is inherited from the father (or more rarely when there are two copies of the gene from the moth ...
Meiosis PowerPoint Notes
Meiosis PowerPoint Notes

... 1. Performed by the two new cells produced in  each of the new haploid cell’s chromosomes contains 2 unique chromatids 2. DNA does replicate! 3. Prophase through cytokinesis occurs. ...
Disease
Disease

... 1. Performed by the two new cells produced in  each of the new haploid cell’s chromosomes contains 2 unique chromatids 2. DNA does replicate! 3. Prophase through cytokinesis occurs. ...
alleles - Jordan High School
alleles - Jordan High School

... • Cells containing both sets of chromosomes are diploid (2N) • Cells containing single set of chromosomes are haploid (N) ...
ChromoSock Mitosis Instructor Protocol
ChromoSock Mitosis Instructor Protocol

... mother and the other half from father. Point out that although the socks may appear slightly different, one can easily determine which two should be paired. Ask students if they can identify which of each pair of chromosomes came from the father and which came from the mother. Answer: No. Ask s ...
L8 cells PPt - Moodle
L8 cells PPt - Moodle

...  XY = male  XX = female  Male determines sex of child (always an X chromosome from mother)  X chromosome larger than Y  Alleles on X chromosome may not have equivalent on Y ...
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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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