Download 22q11.2 Deletion Syndrome - A Bibliography and Dictionary by Philip M. Parker PDF

By Philip M. Parker

In March 2001, the nationwide Institutes of wellbeing and fitness issued the next caution: "The variety of sites supplying health-related assets grows on a daily basis. Many websites offer beneficial details, whereas others can have info that's unreliable or misleading." moreover, a result of speedy elevate in Internet-based info, many hours should be wasted looking out, choosing, and printing. given that basically the smallest fraction of data facing 22q11.2 deletion syndrome is listed in se's, corresponding to www.google.com or others, a non-systematic method of net learn may be not just time eating, but additionally incomplete. This booklet was once created for doctors, scholars, and contributors 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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Extra resources for 22q11.2 Deletion Syndrome - A Bibliography and Dictionary for Physicians, Patients, and Genome Researchers

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A variety of genes are involved in the control of cell growth and division. The cell cycle is the cell’s way of replicating itself in an organized, step-by-step fashion. Tight regulation of this process ensures that a dividing cell’s DNA is copied properly, any errors in the DNA are repaired, and each daughter cell receives a full set of chromosomes. The cycle has checkpoints (also called restriction points), which allow certain genes to check for mistakes and halt the cycle for repairs if something goes wrong.

Source: The American Journal of Psychiatry. db=pubmed&cmd=Retrieve&dopt=A bstractPlus&list_uids=15930057&query_hl=1&itool=pubmed_docsum • New perspectives on use of thymic factors in immune deficiency. Author(s): Cunningham-Rundles S, Harbison M, Guirguis S, Valacer D, Chretien PB. Source: Annals of the New York Academy of Sciences. db=pubmed&cmd=Retrieve&dopt=A bstractPlus&list_uids=8080216&query_hl=1&itool=pubmed_docsum • Transition from latent to overt hypoparathyroidism in a child with CATCH 22.

De novo mutations may explain genetic disorders in which an affected child has a mutation in every cell, but has no family history of the disorder. Acquired (or somatic) mutations occur in the DNA of individual cells at some time during a person’s life. These changes can be caused by environmental factors such as ultraviolet radiation from the sun, or can occur if a mistake is made as DNA copies itself during cell division. Acquired mutations in somatic cells (cells other than sperm and egg cells) cannot be passed on to the next generation.

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