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The Encyclopedia of Genetic Disorders and Birth Defects, 3rd Edition (Facts on File Library of Health and Living)

معرفی کتاب «The Encyclopedia of Genetic Disorders and Birth Defects, 3rd Edition (Facts on File Library of Health and Living)» نوشتهٔ James Wynbrandt and Mark D. Ludman, M.D., F.R.C.P.C، منتشرشده توسط نشر Facts On File در سال 2008. این کتاب در فرمت pdf، زبان انگلیسی ارائه شده است.

This encyclopaedia provides data and qualified clinical information on genetic disorders. It is reckoned that one in ten babies born throughout the world suffer a genetic disease or birth defect, and, if so-called "late-onset" genetic disorders are counted, six in ten can be considered to suffer from some form of genetically-influenced disorder. The encyclopaedia's aim is to provide concise information in A to Z format for practitioners, researchers and concerned individuals alike. It covers all statistically significant afflictions, their original identification and "history", information on prognosis, availability of prenatal detection, biochemical and molecular bases, discussion of the various diagnostic and screening techniques and data on risk groups and mutogenic agents. All the genetic terminology necessary for a full understanding of the subject is defined, and each entry reflects contemporary published research in its field. In recent years, doctors and scientists have made great strides in increasing our knowledge of hundreds of genetic disorders. Many serious disorders have now been identified as having a genetic basis, and treatment for birth defects has improved substantially."The Encyclopedia of Genetic Disorders and Birth Defects, Third Edition" offers lay readers and professionals alike the most comprehensive single-volume reference to congenital disorders and birth defects. This accessible volume contains more than 1,000 expertly written entries - including more than 135 new entries and more than 60 revised entries, extensive appendixes providing updated tables of statistics and directories of service and support groups, and a concise introductory history of human genetics. This new edition has been extensively updated to reflect the most current research. -- Publisher's description

incl. Historical Data, Information On Prognosis & Mode Of Inheritance, Prenatal Diagnosis & Carrier Screening, Etc.

school Library Journal

ya-- A Readable Book With A Wealth Of Information For Students Of Biology And Psychology. It Has Well-written And Clearly Cited Source Entries, And Gives Excellent Background On Genetic Problems. Also Included Are Descriptions Of Centers For Genetic Study And Listings Of Available Resources For Those Interested In Locating Services For People With Birth Defects. Charts And Graphs Enable Readers To Compare Statistical Information.

Includes numerous entries that describe the condition, its prognosis, prevalence, mode of inheritance and the availability of carrier screening and prenatal diagnosis. Entries for subjects and terminology important to genetic disorders and congenital anomalies are also included. Offers lay readers and professionals alike a reference to congenital disorders and birth defects. This volume contains more than 1,000 entries, appendixes providing tables of statistics and directories of service and support groups, and an introductory history of human genetics. Provides information on the history, prognosis, availability of prenatal detection, and symptoms of hundreds of genetically transmitted conditions
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