Genetic Screening: From Newborns to DNA Typing: Proceedings of the Workshop on Genetic Screening Held at La Sapiniere, Quebec (Canada) 13th-14th October 1989 for the Bi-Annual Meeting Between the Quebec Network of Genetic Medicine and the New England R... Bartha Maria Knoppers

ISBN: 9780444812032

Published: December 31st 1990

Hardcover


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Genetic Screening: From Newborns to DNA Typing: Proceedings of the Workshop on Genetic Screening Held at La Sapiniere, Quebec (Canada) 13th-14th October 1989 for the Bi-Annual Meeting Between the Quebec Network of Genetic Medicine and the New England R...  by  Bartha Maria Knoppers

Genetic Screening: From Newborns to DNA Typing: Proceedings of the Workshop on Genetic Screening Held at La Sapiniere, Quebec (Canada) 13th-14th October 1989 for the Bi-Annual Meeting Between the Quebec Network of Genetic Medicine and the New England R... by Bartha Maria Knoppers
December 31st 1990 | Hardcover | PDF, EPUB, FB2, DjVu, audiobook, mp3, RTF | | ISBN: 9780444812032 | 6.23 Mb

Dramatic advances in recombinant DNA technology are about to bring fundamental changes in genetic screening. As clinically oriented researchers pursue dozens of disease genes, basic scientists dazzle us with new technologies, one of the mostMoreDramatic advances in recombinant DNA technology are about to bring fundamental changes in genetic screening.

As clinically oriented researchers pursue dozens of disease genes, basic scientists dazzle us with new technologies, one of the most important being the polymerase chain reaction. The questions accompanying screening scenarios seem to amplify at a rate approaching that of the polymerase chain reaction.

Genetic Screening: From Newborns to DNA Typing arrives at a crucial moment to help us confront these and many other questions. It is the work product of two dozen leading authorities in the field of newborn screening who gathered to focus their thoughts intensively on the present state of screening and to formulate principles to guide the practice of neonatal screening in the next decade.

The book is logically organized and presents much valuable material, examines the more recent experiences in screening for congenital diseases, ascertaining HIV seroprevalence, and raises important ethical and legal questions. The volume is an admirable conception and will undoubtedly be of interest to all involved with genetic testing.



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