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Haploid (__)
Haploid (__)

... Homologous Chromosomes---Karyotype: Autosomes: Sex Chromosomes: ...
Human Genetics - Biology Department
Human Genetics - Biology Department

...  Remember:  Have 23 pairs  1 of each pair came from mom  1 of each pair came from dad ...
What are chromosomes?
What are chromosomes?

... Most are rod-shaped. In body cells, chromosomes are found in Body cells are all the cells except sperm and egg cells. Each kind of organism has a specific number of chromosomes. For a example, every body cell of a fruit fly has S chromosomes (4 pairs); human has 46 (23 pairs); a garden pea has 14 (7 ...
Chapter 13 - dewhozitz.net
Chapter 13 - dewhozitz.net

... Dominant -> visible result Recessive -> something missing ...
It`s All in the Genes
It`s All in the Genes

... may be due to Achoo syndrome (an acronym for “autosomal dominant compelling helioophthalmic outburst” syndrome). Figure 24A illustrates some more common genetic traits. ■ ...
Genetics
Genetics

... A hybrid; Different combination of alleles resulting in the dominant trait showing. (one upper case and one lower case letter) 15. What is the difference between phenotype and genotype? The phenotype is what the gene combination looks like. The 16. What is a Punnett Square use for? To find the proba ...
chapter 15 chromosomal basis of inheritance
chapter 15 chromosomal basis of inheritance

... Genetic recombination – the production of offspring with new combinations of traits inherited from two parents. 2 types of offspring can be produced:  Parental types – offspring matching a parental phenotype.  Recombinants – offspring that do not match either parent’s phenotype. The further apart ...
LP - Columbia University
LP - Columbia University

... components not lost, just taken apart into subunits. (Lego castle disassembled -- will be reassembled into two smaller castles after division). 3. Spindle -- have set of fibers attached to chromosomes (and to structures at poles). Assembly of spindle is temporary -fiber components are not new, but w ...
Name - mybiologyclass
Name - mybiologyclass

... 7. Mating / Fertilization. Gently push the like-sized chromosomes toward each other at point halfway between you, pairing them up according to size and number. This represents the moment when a new human potential is reached. A totally unique human is conceived! ...
MITOSIS REVIEW
MITOSIS REVIEW

... • treat disorders like spinal damage, Parkinson’s disease, leukemia • Make heart and nerve tissue in the lab ...
Blood group
Blood group

... shape/identical in appearance OR XX chromosomes present/two X chromosomes present OR No Y chromosome/no XY chromosomes 1.13.3 47/46 +1 /23 pairs +1 - Down's syndrome/Trisomy 21 ...
Document
Document

... B. all sons are normal and all daughters are carriers. C. half of sons are normal and half are hemophilic; all daughters are carriers. D. all daughters are normal and all sons are carriers. E. half of daughters are hemophilic and half of daughters are carriers; all sons are normal. ...
The Human Genome Project
The Human Genome Project

... Summary of Studying the Human Genome  Scientists can read the base sequences in DNA with tools that cut, separate, and replicate DNA base by base.  The Human Genome Project was an effort to sequence base pairs of human DNA and identify human genes. ...
1-. During the first meiotic division (meiosis 1), (A) homologous
1-. During the first meiotic division (meiosis 1), (A) homologous

genetics review sheet
genetics review sheet

... shown in the figure. A family has eight children. Six children have second toes that are longer than the big toe. Two children have second toes that are shorter than the big toe. What are the most likely genotypes of the parents? ...
800X400 pixel file here
800X400 pixel file here

... gene aberrations (mistakes). Still, most single gene mistakes go unnoticed. (Special note: many single gene dysfunction can be determined by chemical analysis of the cells recovered during amniocentesis.) One common use of karyotyping would be in conjunction with amniocentesis. This is of significan ...
Name - O. Henry Science
Name - O. Henry Science

Meiosis - My Haiku
Meiosis - My Haiku

... individual traits. The genes do not just float around in a cell. They are lined up on chromosomes. A typical chromosome can have thousands of genes. If you took a cell from one of Mendel’s pea plants, you would see that it has 14 chromosomes, or seven pairs. In the body cells of most living things, ...
Chromosomes and Inheritance - 1 Chromosome Theory of
Chromosomes and Inheritance - 1 Chromosome Theory of

... We are comfortable with the idea that there are differences in the sex chromosomes. There are differences in parental autosomes, too. In some cases, it makes a difference which gamete provided the chromosome. Imprinting is gender specific and appears to be caused by actions on chromosomes during the ...
(FA-SAT) in a Cat Fibrosarcoma Might Be Related to Chromosomal
(FA-SAT) in a Cat Fibrosarcoma Might Be Related to Chromosomal

... numerical chromosomal alterations. Further segmental chromosomal gains and losses come from structural chromosomal alterations, including reciprocal and nonreciprocal translocations, homogeneously staining regions, amplifications, insertions, and deletions. Structural alterations may result in a fur ...
Heredity – the passing of traits from parents to offspring
Heredity – the passing of traits from parents to offspring

... Heredity – the passing of traits from parents to offspring. Genetics – the study of heredity DNA – cellular material with all the information about what traits a living thing may have Chromosome – thread like structures that organize DNA, each chromosome is a long DNA molecule (about 1.5 meters!) Ge ...
Genetics Class Notes 2017
Genetics Class Notes 2017

... Amniocentesis-A technique in which amniotic fluid and embryonic cells are retrieved and analyzed for genetic defects. Cells are cultured and examined microscopically to find the point of cell division A photo of the chromosomes is taken which is called a Karyotype-A photo of the chromosomes arranged ...
Name - Humble ISD
Name - Humble ISD

... 1. Nondisjunction - Abnormal numbers of chromosomes in ________________________ result in genetic disorders called ____________________________________. This must often is a result of ___________________________, which means __________________________________________. In nondisjunction, a chromosome ...
Nature vs. Nurture
Nature vs. Nurture

... • DNA (deoxyribonucleic acid): special molecule that contains the ___________________ of the organism • Contain genetic _____ for building the _________ that make up _________________ • Ex. hair coloring, muscle, skin • Chromosomes: tightly wound strand of _____________ __________ or DNA • Genes: se ...
Lecture 1. The subject and the main tasks of Medical Genetics
Lecture 1. The subject and the main tasks of Medical Genetics

... he was also assigned to tend the gardens and grow vegetables for the monks to eat. ...
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Chromosome



A chromosome (chromo- + -some) is a packaged and organized structure containing most of the DNA of a living organism. It is not usually found on its own, but rather is complexed with many structural proteins called histones as well as associated transcription (copying of genetic sequences) factors and several other macromolecules. Two ""sister"" chromatids (half a chromosome) join together at a protein junction called a centromere. Chromosomes are normally visible under a light microscope only when the cell is undergoing mitosis. Even then, the full chromosome containing both joined sister chromatids becomes visible only during a sequence of mitosis known as metaphase (when chromosomes align together, attached to the mitotic spindle and prepare to divide). This DNA and its associated proteins and macromolecules is collectively known as chromatin, which is further packaged along with its associated molecules into a discrete structure called a nucleosome. Chromatin is present in most cells, with a few exceptions - erythrocytes for example. Occurring only in the nucleus of eukaryotic cells, chromatin composes the vast majority of all DNA, except for a small amount inherited maternally which is found in mitochondria. In prokaryotic cells, chromatin occurs free-floating in cytoplasm, as these cells lack organelles and a defined nucleus. The main information-carrying macromolecule is a single piece of coiled double-stranded DNA, containing many genes, regulatory elements and other noncoding DNA. The DNA-bound macromolecules are proteins, which serve to package the DNA and control its functions. Chromosomes vary widely between different organisms. Some species such as certain bacteria also contain plasmids or other extrachromosomal DNA. These are circular structures in the cytoplasm which contain cellular DNA and play a role in horizontal gene transfer.Compaction of the duplicated chromosomes during cell division (mitosis or meiosis) results either in a four-arm structure (pictured to the right) if the centromere is located in the middle of the chromosome or a two-arm structure if the centromere is located near one of the ends. Chromosomal recombination during meiosis and subsequent sexual reproduction plays a vital role in genetic diversity. If these structures are manipulated incorrectly, through processes known as chromosomal instability and translocation, the cell may undergo mitotic catastrophe and die, or it may unexpectedly evade apoptosis leading to the progression of cancer.In prokaryotes (see nucleoids) and viruses, the DNA is often densely packed and organized. In the case of archaea by homologs to eukaryotic histones, in the case of bacteria by histone-like proteins. Small circular genomes called plasmids are often found in bacteria and also in mitochondria and chloroplasts, reflecting their bacterial origins.
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