Carnitine Palmitoyltransferase I Deficiency - A Bibliography by Philip M. Parker

By Philip M. Parker

In March 2001, the nationwide Institutes of well-being issued the next caution: "The variety of websites providing health-related assets grows on a daily basis. Many websites supply priceless details, whereas others could have info that's unreliable or misleading." in addition, as a result of the speedy elevate in Internet-based details, many hours could be wasted looking out, deciding on, and printing. considering the fact that basically the smallest fraction of data facing Carnitine palmitoyltransferase I deficiency is listed in se's, equivalent to www.google.com or others, a non-systematic method of net study should be not just time eating, but in addition incomplete. This ebook was once created for doctors, scholars, and individuals of most of the people who are looking to behavior scientific learn utilizing the main complicated instruments on hand and spending the smallest amount of time doing so.

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Forensic testing uses DNA sequences to identify an individual for legal purposes. Unlike the tests described above, forensic testing is not used to detect gene mutations associated with disease. This type of testing can identify crime or catastrophe victims, rule out or implicate a crime suspect, or establish biological relationships between people (for example, paternity). 42 Carnitine Palmitoyltransferase I Deficiency How Is Genetic Testing Done? Once a person decides to proceed with genetic testing, a medical geneticist, primary care doctor, specialist, or nurse practitioner can order the test.

Unlike the tests described above, forensic testing is not used to detect gene mutations associated with disease. This type of testing can identify crime or catastrophe victims, rule out or implicate a crime suspect, or establish biological relationships between people (for example, paternity). 42 Carnitine Palmitoyltransferase I Deficiency How Is Genetic Testing Done? Once a person decides to proceed with genetic testing, a medical geneticist, primary care doctor, specialist, or nurse practitioner can order the test.

Mono-” is Greek for “one”; people with monosomy have one copy of a particular chromosome in each cell instead of the normal two copies. Turner syndrome is a condition caused by monosomy. Women with Turner syndrome are often missing one copy of the X chromosome in every cell, for a total of 45 chromosomes per cell. Chromosomal disorders can also be caused by changes in chromosome structure. These changes are caused by the breakage and reunion of chromosome segments when an egg or sperm cell is formed or in early fetal development.

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