By Philip M. Parker
In March 2001, the nationwide Institutes of future health issued the next caution: "The variety of sites supplying health-related assets grows on a daily basis. Many websites offer important details, whereas others could have details that's unreliable or misleading." moreover, due to the speedy bring up in Internet-based info, many hours may be wasted looking, picking, and printing. seeing that in basic terms the smallest fraction of data facing Andersen-Tawil syndrome is listed in se's, similar to www.google.com or others, a non-systematic method of net study will be not just time eating, but additionally incomplete. This e-book used to be created for doctors, scholars, and participants of most of the people who are looking to behavior clinical learn utilizing the main complicated instruments to be had and spending the smallest amount of time doing so.
Read or Download Andersen-Tawil Syndrome - A Bibliography and Dictionary for Physicians, Patients, and Genome Researchers PDF
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Additional resources for Andersen-Tawil Syndrome - A Bibliography and Dictionary for Physicians, Patients, and Genome Researchers
What Is Direct-to-Consumer Genetic Testing? Traditionally, genetic tests have been available only through healthcare providers such as physicians, nurse practitioners, and genetic counselors. Healthcare providers order the appropriate test from a laboratory, collect and send the samples, and interpret the test results. Direct-to-consumer genetic testing refers to genetic tests that are marketed directly to consumers via television, print advertisements, or the Internet. This form of testing, which is also known as at-home genetic testing, provides access to a person’s genetic information without necessarily involving a doctor or insurance company in the process.
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. For specific information about how genes are named, refer to the HGNC’s Guidelines for Human Gene Nomenclature. Genetics Home Reference describes genes using the HGNC’s official gene names and gene symbols. Genetics Home Reference frequently presents the symbol and name separated with a colon (for example, FGFR4: Fibroblast growth factor receptor 4).
Cystic fibrosis, sickle cell anemia X-linked dominant X-linked dominant disorders are caused by mutations in genes on the X chromosome. Females are more frequently affected than males, and the chance of passing on an X-linked dominant disorder differs between men and women. Families with an X-linked dominant disorder often have both affected males and 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).