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Karyotypes: Diagnosing Chromosome Disorders HASP Medical Biology Lab 17 Background/Introduction DNA, Genes, and Chromosomes All cells contain genetic information in the form of deoxyribonucleic acid(DNA)
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How to fill out karyotypes diagnosing chromosome disorders

01
To fill out karyotypes diagnosing chromosome disorders, follow these steps:
02
Obtain a sample of cells from the individual's body, such as blood or tissue.
03
Culture the cells in a laboratory to allow them to divide and grow.
04
Arrest the cell division process at metaphase, when the chromosomes are most condensed and visible.
05
Stain the chromosomes using a dye to enhance their visibility under a microscope.
06
Photograph the stained chromosomes using a camera attached to the microscope.
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Identify and arrange the chromosomes in pairs according to their size, centromere position, and banding pattern.
08
Analyze the karyotype to determine any abnormalities or variations in the number, structure, or arrangement of chromosomes.
09
Compare the karyotype to a standard reference to identify any chromosome disorders or abnormalities.
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Document the findings and provide a detailed report of the karyotype analysis.

Who needs karyotypes diagnosing chromosome disorders?

01
Karyotypes diagnosing chromosome disorders are often needed by medical professionals, including:
02
- Geneticists: to evaluate genetic conditions and identify chromosomal abnormalities.
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- Obstetricians: to screen for fetal genetic disorders or to investigate the cause of recurrent miscarriages.
04
- Pediatricians: to diagnose and manage genetic disorders in children.
05
- Hematologists: to assess certain blood disorders related to chromosomal abnormalities.
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- Oncologists: to identify specific chromosomal changes in cancer cells.
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- Researchers: to study and understand the role of chromosomes in various diseases and conditions.

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