Download 22q11.2 Deletion Syndrome - A Bibliography and Dictionary by Philip M. Parker PDF

By Philip M. Parker

In March 2001, the nationwide Institutes of future health issued the subsequent caution: "The variety of websites supplying health-related assets grows on a daily basis. Many websites supply priceless details, whereas others can have details that's unreliable or misleading." additionally, as a result of swift elevate in Internet-based details, many hours could be wasted looking, picking out, and printing. when you consider that in basic terms the smallest fraction of knowledge facing 22q11.2 deletion syndrome is listed in se's, corresponding to www.google.com or others, a non-systematic method of web learn might be not just time eating, but additionally incomplete. This e-book used to be created for doctors, scholars, and individuals of most 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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Extra resources for 22q11.2 Deletion Syndrome - A Bibliography and Dictionary for Physicians, Patients, and Genome Researchers

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Nearly every cell in a person’s body has the same DNA. Most DNA is located in the cell nucleus (where it is called nuclear DNA), but a small amount of DNA can also be found in the mitochondria (where it is called mitochondrial DNA or mtDNA). The information in DNA is stored as a code made up of four chemical bases: adenine (A), guanine (G), cytosine (C), and thymine (T). Human DNA consists of about 3 billion bases, and more than 99 percent of those bases are the same in all people. The order, or sequence, of these bases determines the information available for building and maintaining an organism, similar to the way in which letters of the alphabet appear in a certain order to form words and sentences.

These types of RNA help assemble protein building blocks (amino acids) into functioning proteins. What Is a Gene? A gene is the basic physical and functional unit of heredity. Genes, which are made up of DNA, act as instructions to make molecules called proteins. In humans, genes vary in size from a few hundred DNA bases to more than 2 million bases. The Human Genome Project has estimated that humans have between 20,000 and 25,000 genes. Every person has two copies of each gene, one inherited from each parent.

Help Me Understand Genetics 47 • The arm of the chromosome. Each chromosome is divided into two sections (arms) based on the location of a narrowing (constriction) called the centromere. By convention, the shorter arm is called p, and the longer arm is called q. The chromosome arm is the second part of the gene’s address. For example, 5q is the long arm of chromosome 5, and Xp is the short arm of the X chromosome. • The position of the gene on the p or q arm. The position of a gene is based on a distinctive pattern of light and dark bands that appear when the chromosome is stained in a certain way.

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