By Philip M. Parker

ISBN-10: 0497113287

ISBN-13: 9780497113285

ISBN-10: 1429496096

ISBN-13: 9781429496094

In March 2001, the nationwide Institutes of healthiness issued the next caution: "The variety of sites delivering health-related assets grows on a daily basis. Many websites supply invaluable info, whereas others could have info that's unreliable or misleading." additionally, as a result of fast raise in Internet-based info, many hours may be wasted looking out, picking out, and printing. considering that in simple terms the smallest fraction of knowledge facing Andersen-Tawil syndrome is listed in se's, reminiscent of or others, a non-systematic method of net study could be not just time eating, but additionally incomplete. This e-book was once created for doctors, scholars, and contributors of most of the people who are looking to behavior clinical examine utilizing the main complicated instruments on hand and spending the smallest amount of time doing so.

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Additional info for Andersen-Tawil Syndrome - A Bibliography and Dictionary for Physicians, Patients, and Genome Researchers

Sample text

There are two types of cell division: mitosis and meiosis. Most of the time when people refer to “cell division,” they mean mitosis, the process of making new body cells. Meiosis is the type of cell division that creates egg and sperm cells. Mitosis is a fundamental process for life. 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.

Genetics Home Reference consults with experts in the field of medical genetics to provide the current, most accurate name for each disorder. Alternate names are included as synonyms. Naming genes The HUGO Gene Nomenclature Committee (HGNC) designates an official name and symbol (an abbreviation of the name) for each known human gene. Some official gene names include additional information in parentheses, such as related genetic conditions, subtypes of a condition, or inheritance pattern. K. S. National Institutes of Health.

Nonsense mutation: A nonsense mutation is also a change in one DNA base pair. Instead of substituting one amino acid for another, however, the altered DNA sequence prematurely signals the cell to stop building a protein. This type of mutation results in a shortened protein that may function improperly or not at all. • Insertion: An insertion changes the number of DNA bases in a gene by adding a piece of DNA. As a result, the protein made by the gene may not function properly. • Deletion: A deletion changes the number of DNA bases by removing a piece of DNA.

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

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