By Philip M. Parker

ISBN-10: 0497113333

ISBN-13: 9780497113339

ISBN-10: 1429496045

ISBN-13: 9781429496049

In March 2001, the nationwide Institutes of overall healthiness issued the next caution: "The variety of sites providing health-related assets grows each day. Many websites offer important details, whereas others can have info that's unreliable or misleading." in addition, end result of the speedy elevate in Internet-based info, many hours might be wasted looking, determining, and printing. seeing that simply the smallest fraction of data facing Apert syndrome is listed in se's, reminiscent of or others, a non-systematic method of web study might be not just time eating, but additionally incomplete. This publication was once created for doctors, scholars, and individuals of most of the people who are looking to behavior clinical study utilizing the main complex instruments on hand and spending the smallest amount of time doing so.

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Extra resources for Apert Syndrome - A Bibliography and Dictionary for Physicians, Patients, and Genome Researchers

Sample text

Gene mutations occur in two ways: they can be inherited from a parent or acquired during a person’s lifetime. 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.

Db=pubmed&cmd=Retrieve&dopt=A bstractPlus&list_uids=15371125&query_hl=4&itool=pubmed_docsum • Phenotypic diversity in patients with craniosynostoses unrelated to Apert syndrome: the role of fibroblast growth factor receptor gene mutations. Author(s): Ito S, Sekido K, Kanno H, Sato H, Tanaka M, Yamaguchi K, Yamamoto I. Source: Journal of Neurosurgery. db=pubmed&cmd=Retrieve&dopt=A bstractPlus&list_uids=16206730&query_hl=4&itool=pubmed_docsum • Prenatal diagnosis of Apert syndrome with widely separated cranial sutures.

It consists of two major steps: transcription and translation. Together, transcription and translation are known as gene expression. During the process of transcription, the information stored in a gene’s DNA is transferred to a similar molecule called RNA (ribonucleic acid) in the cell nucleus. Both RNA and DNA are made up of a chain of nucleotide bases, but they have slightly different chemical properties. The type of RNA that contains the information for making a protein is called messenger RNA (mRNA) because it carries the information, or message, from the DNA out of the nucleus into the cytoplasm.

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

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