By Philip M. Parker
In March 2001, the nationwide Institutes of future health issued the subsequent caution: "The variety of sites providing health-related assets grows each day. Many websites offer invaluable info, whereas others could have details that's unreliable or misleading." moreover, a result of fast elevate in Internet-based info, many hours will be wasted looking, deciding on, and printing. seeing that merely the smallest fraction of knowledge facing 3-methylglutaconic aciduria is listed in se's, reminiscent of www.google.com or others, a non-systematic method of net examine should be not just time eating, but additionally incomplete. This e-book used to be created for doctors, scholars, and contributors of most of the people who are looking to behavior scientific examine utilizing the main complex instruments to be had and spending the smallest amount of time doing so.
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In March 2001, the nationwide Institutes of overall healthiness issued the subsequent caution: "The variety of sites providing health-related assets grows on a daily basis. Many websites supply useful details, whereas others can have info that's unreliable or deceptive. " additionally, end result of the quick bring up in Internet-based details, many hours could be wasted looking out, identifying, and printing.
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Additional resources for 3-Methylglutaconic Aciduria - A Bibliography and Dictionary for Physicians, Patients, and Genome Researchers
A woman passes on one or the other of her X chromosomes to each child. Therefore, a woman with an X-linked dominant disorder has a 50 percent chance of having an affected daughter or son with each pregnancy. • X-linked recessive inheritance: Because of the difference in sex chromosomes, the probability of passing on an X-linked recessive disorder also differs between men and women. The sons of a man with an X-linked recessive disorder will not be affected, and his daughters will carry one copy of the mutated gene.
Doctors who treat families with a particular disorder are often the first to propose a name for the condition. Expert working groups may later revise the name to improve its usefulness. Naming is important because it allows accurate and effective communication about particular conditions, which will ultimately help researchers find new approaches to treatment. Disorder names are often derived from one or a combination of sources: • The basic genetic or biochemical defect that causes the condition (for example, alpha-1 antitrypsin deficiency) • One or more major signs or symptoms of the disorder (for example, sickle cell anemia) • The parts of the body affected by the condition (for example, retinoblastoma) 42 3-Methylglutaconic Aciduria • The name of a physician or researcher, often the first person to describe the disorder (for example, Marfan syndrome, which was named after Dr.
DNA, or deoxyribonucleic acid, is the hereditary material in humans and almost all other organisms. 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.