Read e-book online Achondrogenesis - A Bibliography and Dictionary for PDF

By Philip M. Parker

ISBN-10: 0497113171

ISBN-13: 9780497113179

ISBN-10: 1429496207

ISBN-13: 9781429496209

In March 2001, the nationwide Institutes of overall healthiness issued the subsequent caution: "The variety of websites providing health-related assets grows each day. Many websites offer important info, whereas others could have info that's unreliable or misleading." additionally, as a result of speedy elevate in Internet-based details, many hours could be wasted looking, making a choice on, and printing. when you consider that purely the smallest fraction of data facing Achondrogenesis is listed in se's, similar to www.google.com or others, a non-systematic method of web examine could be not just time eating, but additionally incomplete. This booklet used to be created for doctors, scholars, and participants of most of the people who are looking to behavior scientific study utilizing the main complex instruments to be had and spending the smallest amount of time doing so.

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Extra info for Achondrogenesis - A Bibliography and Dictionary for Physicians, Patients, and Genome Researchers

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2. Help Me Understand Genetics 35 Molecular Location The Human Genome Project, an international research effort completed in 2003, determined the sequence of base pairs for each human chromosome. This sequence information allows researchers to provide a more specific address than the cytogenetic location for many genes. A gene’s molecular address pinpoints the location of that gene in terms of base pairs. For example, the molecular location of the APOE gene on chromosome 19 begins with base pair 50,100,901 and ends with base pair 50,104,488.

A gain or loss of chromosomes from the normal 46 is called aneuploidy. 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. Down syndrome is an example of a condition caused by trisomy—people with Down syndrome typically have three copies of chromosome 21 in each cell, for a total of 47 chromosomes per cell. Monosomy, or the loss of one chromosome from each cell, is another kind of aneuploidy.

Most genes are the same in all people, but a small number of genes (less than 1 percent of the total) are slightly different between people. Alleles are forms of the same gene with small differences in their sequence of DNA bases. These small differences contribute to each person’s unique physical features. Genes are made up of DNA. Each chromosome contains many genes. What Is a Chromosome? In the nucleus of each cell, the DNA molecule is packaged into thread-like structures called chromosomes.

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


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