Get Coffin-Lowry Syndrome - A Bibliography and Dictionary for PDF

By Philip M. Parker

ISBN-10: 0497113538

ISBN-13: 9780497113537

ISBN-10: 1429495847

ISBN-13: 9781429495844

In March 2001, the nationwide Institutes of healthiness issued the subsequent caution: "The variety of sites delivering health-related assets grows each day. Many websites supply important details, whereas others could have info that's unreliable or misleading." moreover, as a result of quick raise in Internet-based info, many hours might be wasted looking out, settling on, and printing. when you consider that purely the smallest fraction of data facing Coffin-Lowry syndrome is listed in se's, similar to www.google.com or others, a non-systematic method of net examine might be not just time eating, but additionally incomplete. This booklet used to be created for doctors, scholars, and contributors of most people who are looking to behavior scientific learn utilizing the main complex instruments to be had and spending the smallest amount of time doing so.

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Additional resources for Coffin-Lowry Syndrome - A Bibliography and Dictionary for Physicians, Patients, and Genome Researchers

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A particular disorder might be described as “running in a family” if more than one person in the family has the condition. Some disorders that affect multiple family members are caused by gene mutations, which can be inherited (passed down from parent to child). Other conditions that appear to run in families are not inherited. Instead, environmental factors Help Me Understand Genetics 43 such as dietary habits or a combination of genetic and environmental factors are responsible for these disorders.

Human cells normally contain 23 pairs of chromosomes, for a total of 46 chromosomes in each cell. A change in the number of chromosomes leads to a chromosomal disorder. These changes can occur during the formation of reproductive cells (eggs and sperm) or in early fetal development. A gain or loss of chromosomes from the normal 46 is called aneuploidy. Help Me Understand Genetics 39 The most common form of aneuploidy is trisomy, or the presence of an extra chromosome in each cell. “Tri-” is Greek for “three”; people with trisomy have three copies of a particular chromosome in each cell instead of the normal two copies.

During mitosis, a cell duplicates all of its contents, including its chromosomes, and splits to form two identical daughter cells. Because this process is so critical, the steps of mitosis are carefully controlled by a number of genes. When mitosis is not regulated correctly, health problems such as cancer can result. The other type of cell division, meiosis, ensures that humans have the same number of chromosomes in each generation. It is a two-step process that reduces the chromosome number by half—from 46 to 23—to form sperm and egg cells.

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Coffin-Lowry Syndrome - A Bibliography and Dictionary for Physicians, Patients, and Genome Researchers by Philip M. Parker


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