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Philip M. Parker's Pendred Syndrome - A Bibliography and Dictionary for PDF

By Philip M. Parker

ISBN-10: 049711271X

ISBN-13: 9780497112714

ISBN-10: 1429496673

ISBN-13: 9781429496674

In March 2001, the nationwide Institutes of health and wellbeing issued the subsequent caution: "The variety of websites delivering health-related assets grows each day. Many websites supply worthy info, whereas others can have details that's unreliable or misleading." additionally, as a result of the fast elevate in Internet-based info, many hours will be wasted looking out, settling on, and printing. given that merely the smallest fraction of knowledge facing Pendred syndrome is listed in se's, similar to or others, a non-systematic method of web learn will be not just time eating, but in addition incomplete. This e-book was once created for doctors, scholars, and individuals of most people who are looking to behavior clinical study utilizing the main complicated instruments to be had and spending the smallest amount of time doing so.

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Extra info for Pendred Syndrome - A Bibliography and Dictionary for Physicians, Patients, and Genome Researchers

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36 Pendred Syndrome Molecular Location The Human Genome Project, an international research effort completed in 2003, determined the sequence of base pairs for each human chromosome. This sequence information allows researchers to provide a more specific address than the cytogenetic location for many genes. A gene’s molecular address pinpoints the location of that gene in terms of base pairs. For example, the molecular location of the APOE gene on chromosome 19 begins with base pair 50,100,901 and ends with base pair 50,104,488.

Geneticists use maps to describe the location of a particular gene on a chromosome. One type of map uses the cytogenetic location to describe a gene’s position. The cytogenetic location is based on a distinctive pattern of bands created when chromosomes are stained with certain chemicals. Another type of map uses the molecular location, a precise description of a gene’s position on a chromosome. The molecular location is based on the sequence of DNA building blocks (base pairs) that make up the chromosome.

The chance of developing a genetic condition with codominant inheritance, and the characteristic features of that condition, depend on which versions of the gene are passed from parents to their child. • Mitochondrial inheritance: Mitochondria, which are the energy-producing centers inside cells, each contain a small amount of DNA. Disorders with mitochondrial inheritance result from mutations in mitochondrial DNA. Although mitochondrial Help Me Understand Genetics 51 disorders can affect both males and females, only females can pass mutations in mitochondrial DNA to their children.

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

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