By Philip M. Parker
In March 2001, the nationwide Institutes of wellbeing and fitness issued the subsequent caution: "The variety of websites delivering health-related assets grows each day. Many websites offer worthwhile details, whereas others could have details that's unreliable or misleading." in addition, a result of fast elevate in Internet-based details, many hours could be wasted looking out, identifying, and printing. in view that in basic terms the smallest fraction of knowledge facing Cornelia de Lange syndrome is listed in se's, corresponding to www.google.com or others, a non-systematic method of net study will be not just time eating, but in addition incomplete. This ebook used to be created for doctors, scholars, and contributors of most of the people who are looking to behavior scientific learn utilizing the main complex instruments to be had and spending the smallest amount of time doing so.
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Extra resources for Cornelia de Lange Syndrome - A Bibliography and Dictionary for Physicians, Patients, and Genome Researchers
These complex disorders are influenced by a combination of genetic factors, environmental conditions, and lifestyle choices. A family history also can provide information about the risk of rarer conditions caused by mutations in a single gene, such as cystic fibrosis and sickle cell anemia. While a family medical history provides information about the risk of specific health concerns, having relatives with a medical condition does not mean that an individual will definitely develop that condition.
Nonsense mutation: A nonsense mutation is also a change in one DNA base pair. Instead of substituting one amino acid for another, however, the altered DNA sequence prematurely signals the cell to stop building a protein. This type of mutation results in a shortened protein that may function improperly or not at all. • Insertion: An insertion changes the number of DNA bases in a gene by adding a piece of DNA. As a result, the protein made by the gene may not function properly. • Deletion: A deletion changes the number of DNA bases by removing a piece of DNA.
Db=pubmed&cmd=Retrieve&dopt=A bstractPlus&list_uids=2709287&query_hl=4&itool=pubmed_docsum • Gastroesophageal reflux and Cornelia de Lange syndrome: typical and atypical symptoms. Author(s): Luzzani S, Macchini F, Valade A, Milani D, Selicorni A. Source: Am J Med Genet A. db=pubmed&cmd=Retrieve&dopt=A bstractPlus&list_uids=12784293&query_hl=4&itool=pubmed_docsum • Gastrointestinal abnormalities in the Cornelia de Lange syndrome. Author(s): Lachman R, Funamura J, Szalay G. Source: The Mount Sinai Journal of Medicine, New York.
Cornelia de Lange Syndrome - A Bibliography and Dictionary for Physicians, Patients, and Genome Researchers by Philip M. Parker