Download e-book for iPad: Molecular Diagnostics, Second Edition by George P. Patrinos, George Patrinos, Wilhelm Ansorge

By George P. Patrinos, George Patrinos, Wilhelm Ansorge

Key gains. comprises cutting-edge innovations for the detection of the underlying genetic heterogeneity resulting in inherited issues. comprises in-depth dialogue of moral and safeguard concerns . Identifies genetically converted organisms (GMO's). Covers forensic research and every-day matters in a diagnostic laboratoryDescriptionThe moment version of Molecular Diagnostics, the single publication facing prognosis on a molecular point, discusses present molecular organic options used to spot the underlying molecular defects in inherited ailment. The ebook delves additional into the primary and short description of the process, by way of examples from the authors' personal services. individuals to the 2/e are recognized specialists of their box, and derive from quite a few disciplines, to make sure breadth and intensity of insurance. Molecular Diagnostics, 2/e , is a wanted source for graduate scholars, researchers, physicians and practising scientists in molecular genetics; pros from comparable backgrounds operating in diagnostic laboratories in academia or undefined, in addition to, educational associations and sanatorium libraries.RELATED TITLES:Trent/Molecular medication, April 2005,$79.95, 0-12-699057-3 Innis (1999) PCR purposes, HB, $89.95,0-12-372185-7, PB, $66.95, Key Features:*Deals solely with the at the moment used molecular biology ideas to spot the underlying molecular illness of inherited diseases*Includes pharmacogenetics and pharmacogenomics in terms of new melanoma therapies*Provies a entire advisor via rising ideas and demonstrates how the on hand mutation screening expertise should be carried out in diagnostic laboratories and supply larger healthcare

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Extra resources for Molecular Diagnostics, Second Edition

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Prenatal diagnosis of b-thalassemia: detection of a single nucleotide mutation in DNA. N. Engl. J. Med. 309, 284–287. , and Gieselmann, V. (1991). Molecular basis of different forms of metachromatic leukodystrophy. N. Engl. J. Med. 324, 18–24. , and Erlich, H. A. (1986). Analysis of enzymatically amplified b-globin and HLADQa DNA with allele-specific oligonucleotide probes. Nature 324, 163–166. A. (1988b). Diagnosis of sickle cell anemia and b-thalassemia with enzymatically amplified DNA and nonradioactive allele-specific oligonucleotide probes.

And Gieselmann, V. (1991). Molecular basis of different forms of metachromatic leukodystrophy. N. Engl. J. Med. 324, 18–24. , and Erlich, H. A. (1986). Analysis of enzymatically amplified b-globin and HLADQa DNA with allele-specific oligonucleotide probes. Nature 324, 163–166. A. (1988b). Diagnosis of sickle cell anemia and b-thalassemia with enzymatically amplified DNA and nonradioactive allele-specific oligonucleotide probes. N. Engl. J. Med. 319, 537–541. , Horn, G. A. (1988a). Primer-directed enzymatic amplification of DNA with a thermostable DNA polymerase.

17, 2503–2516. D. (1989). Direct sequencing of the gene for Maryland/German familial amyloidotic polyneuropathy type II and genotyping by allele-specific enzymatic amplification. Genomics 5, 535–540. , and Wagener, C. (1997). Methods for detection of point mutations: performance and quality assessment. Clin. Chem. 43, 1114–1128. S. (2001). Frequency and ethnic distribution of the common DHCR7 mutation in Smith–Lemli–Opitz syndrome. Am. J. Med. Genet. 102, 383–386. D. (1989). Rapid nonradioactive detection of mutations in the human genome by allele-specific amplification.

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