Download e-book for kindle: 47,XYY Syndrome - A Bibliography and Dictionary for by Philip M. Parker

By Philip M. Parker

ISBN-10: 0497112035

ISBN-13: 9780497112035

ISBN-10: 1429497319

ISBN-13: 9781429497312

In March 2001, the nationwide Institutes of healthiness issued the subsequent caution: "The variety of sites supplying health-related assets grows on a daily basis. Many websites supply invaluable details, whereas others could have details that's unreliable or misleading." in addition, a result of quick bring up in Internet-based details, many hours could be wasted looking, picking out, and printing. for the reason that purely the smallest fraction of data facing 47,XYY syndrome is listed in se's, reminiscent of www.google.com or others, a non-systematic method of web study will be not just time eating, but additionally incomplete. This ebook used to be created for doctors, scholars, and individuals of most people who are looking to behavior clinical examine utilizing the main complicated instruments to be had and spending the smallest amount of time doing so.

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Additional resources for 47,XYY Syndrome - A Bibliography and Dictionary for Physicians, Patients, and Genome Researchers

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How Can Gene Mutations Affect Health and Development? To function correctly, each cell depends on thousands of proteins to do their jobs in the right places at the right times. Sometimes, gene mutations prevent one or more of these proteins from working properly. By changing a gene’s instructions for making a protein, a mutation can cause the protein to malfunction or to be missing entirely. When a mutation alters a protein that plays a critical role in the body, it can disrupt normal development or cause a medical condition.

Only a small percentage of all human genes undergo genomic imprinting. Researchers are not yet certain why some genes are imprinted and others are not. They do know that imprinted genes tend to cluster together in the same regions of chromosomes. Two major clusters of imprinted genes have been identified in humans, one on the short (p) arm of chromosome 11 (at position 11p15) and another on the long (q) arm of chromosome 15 (in the region 15q11 to 15q13). What Is Uniparental Disomy? Uniparental disomy is a factor that influences how some genetic conditions are inherited.

The resulting protein is usually nonfunctional. Insertions, deletions, and duplications can all be frameshift mutations. • Repeat expansion: Nucleotide repeats are short DNA sequences that are repeated a number of times in a row. For example, a trinucleotide repeat is made up of 3-base-pair sequences, and a tetranucleotide repeat is made up of 4-base-pair sequences. A repeat expansion is a mutation that increases the number of times that the short DNA sequence is repeated. This type of mutation can cause the resulting protein to function improperly.

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


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