By Philip M. Parker

ISBN-10: 0497111993

ISBN-13: 9780497111991

ISBN-10: 1429497351

ISBN-13: 9781429497350

In March 2001, the nationwide Institutes of overall healthiness issued the subsequent caution: "The variety of websites supplying health-related assets grows each day. Many websites offer priceless info, whereas others could have details that's unreliable or misleading." in addition, due to the fast raise in Internet-based details, many hours will be wasted looking, opting for, and printing. because in basic terms the smallest fraction of knowledge facing 3-methylcrotonyl-coenzyme A carboxylase deficiency is listed in se's, comparable to www.google.com or others, a non-systematic method of web examine might be not just time eating, but additionally incomplete. This ebook used to be created for doctors, scholars, and contributors of most people who are looking to behavior scientific study utilizing the main complicated instruments on hand and spending the smallest amount of time doing so.

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Extra resources for 3-Methylcrotonyl-Coenzyme A Carboxylase Deficiency - A Bibliography and Dictionary for Physicians, Patients, and Genome Researchers

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Autosomal recessive inheritance: Two unaffected people who each carry one copy of the mutated gene for an autosomal recessive disorder (carriers) have a 25 percent chance with each pregnancy of having a child affected by the disorder. The chance with each pregnancy of having an unaffected child who is a carrier of the disorder is 50 percent, and the chance that a child will not have the disorder and will not be a carrier is 25 percent. • X-linked dominant inheritance: The chance of passing on an X-linked dominant condition differs between men and women because men have one X chromosome and one Y chromosome, while women have two X chromosomes.

Naming Genetic Conditions Genetic conditions are not named in one standard way (unlike genes, which are given an official name and symbol by a formal committee). 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.

By noticing patterns of disorders among relatives, healthcare professionals can determine whether an individual, other family members, or future generations may be at an increased risk of developing a particular condition. A family medical history can identify people with a higher-than-usual chance of having common disorders, such as heart disease, high blood pressure, stroke, certain cancers, and diabetes. These complex disorders are influenced by a combination of genetic factors, environmental conditions, and lifestyle choices.

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3-Methylcrotonyl-Coenzyme A Carboxylase Deficiency - A Bibliography and Dictionary for Physicians, Patients, and Genome Researchers by Philip M. Parker


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