Philip M. Parker's Carnitine-Acylcarnitine Translocase Deficiency - A PDF

By Philip M. Parker

ISBN-10: 0497113481

ISBN-13: 9780497113483

ISBN-10: 1429495898

ISBN-13: 9781429495899

In March 2001, the nationwide Institutes of overall healthiness issued the next caution: "The variety of sites supplying health-related assets grows on a daily basis. Many websites offer invaluable details, whereas others can have details that's unreliable or misleading." additionally, due to the fast bring up in Internet-based info, many hours could be wasted looking out, opting for, and printing. considering the fact that merely the smallest fraction of data facing Carnitine-acylcarnitine translocase deficiency is listed in se's, similar to www.google.com or others, a non-systematic method of net examine should be not just time eating, but in addition incomplete. This publication was once created for doctors, scholars, and individuals of most people who are looking to behavior scientific learn utilizing the main complicated instruments to be had and spending the smallest amount of time doing so.

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Extra resources for Carnitine-Acylcarnitine Translocase Deficiency - A Bibliography and Dictionary for Physicians, Patients, and Genome Researchers

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These meetings are most often in-person visits with individuals or families, but they are occasionally conducted in a group or over the telephone. Help Me Understand Genetics 43 Why Might Someone Have a Genetic Consultation? Individuals or families who are concerned about an inherited condition may benefit from a genetic consultation. The reasons that a person might be referred to a genetic counselor, medical geneticist, or other genetics professional include: • A personal or family history of a genetic condition, birth defect, chromosomal disorder, or hereditary cancer.

Families with an X-linked recessive disorder often have affected males, but rarely affected females, in each generation. A striking characteristic of X-linked inheritance is that fathers cannot pass X-linked traits to their sons (no male-to-male transmission). hemophilia, Fabry disease Codominant In codominant inheritance, two different versions (alleles) of a gene can be expressed, and each version makes a slightly different protein. Both alleles influence the genetic trait or determine the characteristics of the genetic condition.

What Is Genetic Testing? Genetic testing is a type of medical test that identifies changes in chromosomes, genes, or proteins. Most of the time, testing is used to find changes that are associated with inherited disorders. The results of a genetic test can confirm or rule out a suspected genetic condition or help determine a person’s chance of developing or passing on a genetic disorder. Several hundred genetic tests are currently in use, and more are being developed. Genetic testing is voluntary.

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Carnitine-Acylcarnitine Translocase Deficiency - A Bibliography and Dictionary for Physicians, Patients, and Genome Researchers by Philip M. Parker


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