By Philip M. Parker
In March 2001, the nationwide Institutes of healthiness issued the subsequent caution: "The variety of sites supplying health-related assets grows each day. Many websites supply useful details, whereas others can have details that's unreliable or misleading." additionally, end result of the speedy elevate in Internet-based info, many hours might be wasted looking, settling on, and printing. due to the fact purely the smallest fraction of data facing alkaptonuria is listed in se's, corresponding to www.google.com or others, a non-systematic method of net 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 learn 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 healthiness issued the subsequent caution: "The variety of websites supplying health-related assets grows on a daily basis. Many websites offer useful details, whereas others could have info that's unreliable or deceptive. " additionally, as a result fast bring up in Internet-based info, many hours should be wasted looking out, picking out, and printing.
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Additional resources for Alkaptonuria - A Bibliography and Dictionary for Physicians, Patients, and Genome Researchers
Mutations that are passed from parent to child are called hereditary mutations or germline mutations (because they are present in the egg and sperm cells, which are also called germ cells). This type of mutation is present throughout a person’s life in virtually every cell in the body. Mutations that occur only in an egg or sperm cell, or those that occur just after fertilization, are called new (de novo) mutations. 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.
Source: Clinica Chimica Acta; International Journal of Clinical Chemistry. db=pubmed&cmd=Retrieve&dopt=A bstractPlus&list_uids=5022110&query_hl=13&itool=pubmed_docsum • The Lancet. The incidence of alkaptonuria: a study in chemical individuality. Author(s): Garrod AE. Source: Nutrition Reviews. db=pubmed&cmd=Retrieve&dopt=A bstractPlus&list_uids=1091883&query_hl=13&itool=pubmed_docsum • The molecular basis of alkaptonuria. Author(s): Fernandez-Canon JM, Granadino B, Beltran-Valero de Bernabe D, Renedo M, Fernandez-Ruiz E, Penalva MA, Rodriguez de Cordoba S.
Source: The Tohoku Journal of Experimental Medicine. db=pubmed&cmd=Retrieve&dopt=A bstractPlus&list_uids=3810644&query_hl=13&itool=pubmed_docsum • Diagnosis of alkaptonuria in children. Author(s): Srsen S, Srsnova K. Source: Padiatr Padol. db=pubmed&cmd=Retrieve&dopt=A bstractPlus&list_uids=460920&query_hl=13&itool=pubmed_docsum 22 Alkaptonuria • Discoloration of the teeth in alkaptonuria (ochronosis) and parkinsonism. Author(s): Siekert RG, Gibilisco JA. Source: Oral Surg Oral Med Oral Pathol.