Table of contents

1. Introduction to Genetics51m
2. Mendel's Laws of Inheritance3h 37m
3. Extensions to Mendelian Inheritance2h 41m
4. Genetic Mapping and Linkage2h 28m
5. Genetics of Bacteria and Viruses1h 21m
6. Chromosomal Variation1h 48m
7. DNA and Chromosome Structure56m
8. DNA Replication1h 10m
9. Mitosis and Meiosis1h 34m
10. Transcription1h 0m
11. Translation58m
12. Gene Regulation in Prokaryotes1h 19m
13. Gene Regulation in Eukaryotes44m
14. Genetic Control of Development44m
15. Genomes and Genomics1h 50m
16. Transposable Elements47m
17. Mutation, Repair, and Recombination1h 6m
18. Molecular Genetic Tools19m
- Genetic Cloning
  9m
- Methods for Analyzing DNA
  9m
19. Cancer Genetics29m
- Overview of Cancer
  21m
- Cancer Mutations
  7m
20. Quantitative Genetics1h 26m
21. Population Genetics50m
- Hardy Weinberg
  19m
- Allelic Frequency Changes
  31m
22. Evolutionary Genetics29m

6. Chromosomal Variation

Chromosomal Mutations: Aneuploidy

Genetics

6. Chromosomal Variation

Chromosomal Mutations: Aneuploidy

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1:42 minutes

Problem B.11b

Textbook Question

The most common reason a physician might recommend that a woman have maternal serum screening and a karyotype analysis is concern that her fetus may have Down syndrome. Go to the OMIM website at www.ncbi.nlm.nih.gov/omim and look up Down syndrome (OMIM 190685).
Look at the 'Mapping' and 'Molecular Genetics' sections and describe what is meant by the Down syndrome critical region (DSCR).

Verified step by step guidance

Begin by understanding that Down syndrome is a genetic disorder caused primarily by the presence of an extra copy of chromosome 21, known as trisomy 21.

Visit the OMIM website and search for the entry with the identifier 190685, which corresponds to Down syndrome, to access detailed genetic information.

Locate the 'Mapping' section on the OMIM page to find information about the specific regions on chromosome 21 that are associated with the features of Down syndrome.

Next, read the 'Molecular Genetics' section to understand the concept of the Down syndrome critical region (DSCR), which refers to a specific segment of chromosome 21 believed to contain the genes most responsible for the characteristic traits of Down syndrome.

Summarize that the DSCR is a defined portion of chromosome 21 where gene dosage imbalance (due to trisomy) leads to the phenotypic manifestations of Down syndrome, highlighting its importance in research and diagnosis.

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Key Concepts

Here are the essential concepts you must grasp in order to answer the question correctly.

Down Syndrome and Its Genetic Basis

Down syndrome is a genetic disorder caused primarily by trisomy of chromosome 21, leading to intellectual disability and characteristic physical features. Understanding its genetic basis involves recognizing that an extra copy of chromosome 21 disrupts normal development, which is why prenatal screening and karyotyping are used to detect this condition.

Down Syndrome Critical Region (DSCR)

The Down Syndrome Critical Region (DSCR) is a specific segment on chromosome 21 believed to contain genes responsible for many of the features of Down syndrome. Identifying this region helps researchers focus on key genes whose overexpression contributes to the syndrome’s phenotype, aiding in understanding and potential therapies.

Maternal Serum Screening and Karyotype Analysis

Maternal serum screening measures specific proteins and hormones in a pregnant woman's blood to assess the risk of chromosomal abnormalities like Down syndrome. Karyotype analysis involves examining fetal chromosomes directly to confirm the presence of trisomy 21, providing a definitive diagnosis.

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