By Philip M. Parker
In March 2001, the nationwide Institutes of wellbeing and fitness issued the subsequent caution: "The variety of sites providing health-related assets grows each day. Many websites offer invaluable info, whereas others could have info that's unreliable or misleading." in addition, due to the speedy bring up in Internet-based details, many hours could be wasted looking out, determining, and printing. on account that simply the smallest fraction of knowledge facing Andersen-Tawil syndrome is listed in se's, akin to www.google.com or others, a non-systematic method of web examine should be not just time eating, but additionally incomplete. This booklet used to be created for doctors, scholars, and participants of most of the people who are looking to behavior scientific study utilizing the main complex instruments on hand and spending the smallest amount of time doing so.
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In March 2001, the nationwide Institutes of well-being issued the next caution: "The variety of websites delivering health-related assets grows on a daily basis. Many websites supply beneficial info, whereas others could have info that's unreliable or deceptive. " additionally, as a result fast bring up in Internet-based info, many hours may be wasted looking out, opting for, and printing.
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Extra info for Andersen-Tawil Syndrome - A Bibliography and Dictionary for Physicians, Patients, and Genome Researchers
Reduced penetrance probably results from a combination of genetic, environmental, and lifestyle factors, many of which are unknown. This phenomenon can make it challenging for genetics professionals to interpret a person’s family medical history and predict the risk of passing a genetic condition to future generations. Variable Expressivity Although some genetic disorders exhibit little variation, most have signs and symptoms that differ among affected individuals. Variable expressivity refers to the range of signs and 38 Andersen-Tawil Syndrome symptoms that can occur in different people with the same genetic condition.
What Is Uniparental Disomy? Uniparental disomy is a factor that influences how some genetic conditions are inherited. Uniparental disomy (UPD) occurs when a person receives two copies of a chromosome, or part of a chromosome, from one parent and no copies from the other parent. UPD can occur as a random event during the formation of egg or sperm cells or may happen in early fetal development. In many cases, UPD likely has no effect on health or development. Because most genes are not imprinted, it doesn’t matter if a person inherits both copies from one parent instead of one copy from each parent.
The addition and removal of methyl groups can be used to control the activity of genes. 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).
Andersen-Tawil Syndrome - A Bibliography and Dictionary for Physicians, Patients, and Genome Researchers by Philip M. Parker