Alkaptonuria - A Bibliography and Dictionary for Physicians, by Philip M. Parker PDF

By Philip M. Parker

ISBN-10: 049711321X

ISBN-13: 9780497113216

ISBN-10: 1429496169

ISBN-13: 9781429496162

In March 2001, the nationwide Institutes of well-being issued the subsequent caution: "The variety of sites supplying health-related assets grows each day. Many websites supply beneficial details, whereas others can have info that's unreliable or misleading." in addition, a result of quick bring up in Internet-based details, many hours will be wasted looking out, making a choice on, and printing. when you consider that merely the smallest fraction of knowledge facing alkaptonuria is listed in se's, resembling www.google.com or others, a non-systematic method of web learn could be not just time eating, but in addition incomplete. This e-book was once created for doctors, scholars, and contributors of most of the people who are looking to behavior scientific examine utilizing the main complicated instruments to be had and spending the smallest amount of time doing so.

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Extra resources for Alkaptonuria - A Bibliography and Dictionary for Physicians, Patients, and Genome Researchers

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Source: Surg Forum. db=pubmed&cmd=Retrieve&dopt=A bstractPlus&list_uids=401217&query_hl=13&itool=pubmed_docsum 30 • Alkaptonuria Use of nitisinone in patients with alkaptonuria. Author(s): Suwannarat P, O'Brien K, Perry MB, Sebring N, Bernardini I, Kaiser-Kupfer MI, Rubin BI, Tsilou E, Gerber LH, Gahl WA. Source: Metabolism: Clinical and Experimental. db=pubmed&cmd=Retrieve&dopt=A bstractPlus&list_uids=15931605&query_hl=13&itool=pubmed_docsum 31 CHAPTER 2. ALTERNATIVE MEDICINE AND ALKAPTONURIA Overview In this chapter, we will begin by introducing you to official information sources on complementary and alternative medicine (CAM) relating to alkaptonuria.

S. National Institutes of Health. The Committee has named more than 13,000 of the estimated 20,000 to 25,000 genes in the human genome. During the research process, genes often acquire several alternate names and symbols. Different researchers investigating the same gene may each give the gene a different name, which can cause confusion. The HGNC assigns a unique name and symbol to each human gene, which allows effective organization of genes in large databanks, aiding the advancement of research.

A particular disorder might be described as “running in a family” if more than one person in the family has the condition. Some disorders that affect multiple family members are caused by gene mutations, which can be inherited (passed down from parent to child). Other conditions that appear to run in families are not inherited. Instead, environmental factors such as dietary habits or a combination of genetic and environmental factors are responsible for these disorders. 52 Alkaptonuria It is not always easy to determine whether a condition in a family is inherited.

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


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