Procedure: You are going to write a summary of and verbally discuss an article of your choosing. See the guidelines below for selecting an appropriate article. Guidelines and grading: 1) Written...

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Procedure:You are going to write a summary of and verbally discuss an article of your choosing. See the guidelines below for selecting an appropriate article.Guidelines and grading:
1) Written Summary

  • The summary must be typed using a 12 pt. font and double spaced.

  • The summary should be
    at least
    two pages but not more than four pages.

  • Do not plagiarize the article but discuss the article’s subject matter in your own words.

  • The summary should include
    at least
    the following information:

  • Identification of the main subjects mentioned in the article and an explanation of what events/phenomena are being discussed in the article

  • The title and author(s) of the article

  • An
    explanation
    of the key terms important for understanding the article. A discussion of these terms should be incorporated into your review of the article.Do not simply list and define the terms separately.

  • A brief discussion of how the article relates to your experience with BIOL 101.

  • The reason you chose the article

  • One question that comes to mind after reading the article


  • In a short paragraph, briefly discuss aspecificexample of how the biological concepts discussed in your article directly relate to your personal life or to a social issue that impacts you.




I would also need an outline with it is it possible?


Answered Same DayJun 28, 2022

Answer To: Procedure: You are going to write a summary of and verbally discuss an article of your choosing. See...

P answered on Jun 28 2022
88 Votes
RARE GENETIC DISORDERS
This article is about the “Rare Genetic Disorders” written by Brendan Borrell
(2020). Rare Diseases are the most commonly observed across the United States and affecting nearly 10 % of the population in the United States. There are more than 7000 types of the rare diseases were reported and of which 80 % accounts for their hereditary, leading to the increased morbidity rates among the children (Borrell, 2020). The parents who are the carriers of the rare genetic disorders were also known as “ rare parents” and there is no cure for the rare genetic disorders and most of them are being managed by some of the potential treatments. A defined diagnosis for the identification of the mutation during the new born screening will takes time and it is one of the biggest challenge in the medical field to identify the disease to the mutation happened.
The studies of Dr. Pelentsov (2016) concluded that the out of 300 rare parents surveyed nearly 40 % of them are being treated for depression and...
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